Innovation Funding Database
Choose Your Area of Innovation:
Advanced Materials & Manufacturing
Aerospace & Spacetech
Agtech & Foodtech
Artificial Intelligence & Machines Learning
Biotech
Cleantech & Climatetech
Cybersecurity
Defensetech & Dual-Use Tech
eXtended Reality
Healthtech
Medtech
Other Tech
Quantum & Photonics
Robotics & Autonomous Systems
CDMRP - Neurofibromatosis Research Program (NFRP)
Deadline: Summer, 2026
Funding Award Size: Up to $3.2m
Description: The FY26 Neurofibromatosis Research Program (NFRP) will fund innovative NF and schwannomatosis research through multiple CDMRP award mechanisms offering up to $3.2M in total funding. Supports early-stage concepts, collaborative research, mentoring academies and high-impact translational projects. Application deadlines have not yet been released.
Below is a brief summary. Please check the full solicitation before applying (link in resources section).
Executive Summary:
The FY26 Neurofibromatosis Research Program (NFRP), administered by the Congressionally Directed Medical Research Programs (CDMRP), is expected to fund multiple award mechanisms supporting innovative, high-impact neurofibromatosis (NF) and schwannomatosis research. The program is specifically focused on improving understanding, diagnosis, treatment and quality of life outcomes for people affected by NF and schwannomatosis, including Service Members, Veterans and their families.
This is currently a pre-announcement. The CDMRP states that funding opportunity announcements will be released on Grants.gov at a later date and will contain official pre-application and application deadlines. At this time, application deadlines are not specified. The program recommends investigators begin planning early.
How much funding would I receive?
The FY26 NFRP includes multiple anticipated award mechanisms with varying funding levels:
Exploration-Hypothesis Development Award
Maximum allowable funding: $160,000 total costs
Maximum performance period: 2 years
Investigator-Initiated Research Award
Maximum allowable funding: $525,000 total costs
Maximum performance period: 3 years
Applications using the Qualified Collaborator or NF Open Science Initiative options may request up to $575,000 total costs
Neurofibromatosis Research Academy – Leadership Award
Maximum allowable funding: $2.4 million total costs
Maximum performance period: 4 years
Neurofibromatosis Research Academy – Scholar Award
Maximum allowable funding: $1.2 million total costs
Maximum performance period: 4 years
Synergistic Idea Award
Maximum allowable funding: $3.2 million total costs
Maximum performance period: 3 years
Total costs include both direct and indirect costs.
What could I use the funding for?
Funding is intended to support innovative and impactful neurofibromatosis and schwannomatosis research projects.
Potential project areas include:
Schwannomatosis and NF2-related research
Biomarker and endpoint validation
Data science applications
Pain and cognitive manifestation research
Sleep-related NF research
Genomics, epigenetics and systems biology
Drug discovery and target identification
Preclinical efficacy studies
Nutritional and environmental modifiers of NF
Health services research
Specific award mechanisms also support:
Early-stage exploratory concepts
Multi-investigator collaborative projects
Early-career investigator development
Multi-institutional mentoring academies
Pilot research projects within academy structures
Clinical trials are not allowed under the listed award mechanisms.
Are there any additional benefits I would receive?
Depending on the award mechanism, applicants may receive additional benefits such as:
Access to collaborative research partnerships
Participation in the NF Open Science Initiative
Intensive mentoring and career development
National networking opportunities
Participation in a virtual NF research academy
Access to NF Consumer Consultant Panels
Multi-institutional collaboration opportunities
The Neurofibromatosis Research Academy mechanisms are specifically designed to support mentorship, networking and long-term investigator development in the NF field.
What is the timeline to apply and when would I receive funding?
The CDMRP released this pre-announcement on April 22, 2026.
Application deadlines are not specified in the pre-announcement. The CDMRP states that official funding opportunity announcements will later be posted on Grants.gov and will include pre-application and application deadlines.
The program requires submission of a pre-application through eBRAP prior to full application submission.
Periods of performance vary by award mechanism:
2 years for Exploration-Hypothesis Development Awards
3 years for Investigator-Initiated Research Awards
4 years for Academy Leadership Awards
4 years for Academy Scholar Awards
3 years for Synergistic Idea Awards
The solicitation does not specify anticipated award start dates or funding disbursement timelines.
Where does this funding come from?
Funding comes from the FY26 Defense Appropriations Act through the Department of Defense Congressionally Directed Medical Research Programs (CDMRP), managed within the Defense Health Agency Research and Development – Medical Research and Development Command (DHA R&D-MRDC).
Who is eligible to apply?
Eligibility depends on the award mechanism.
Exploration-Hypothesis Development Award:
Investigators at all career levels
Includes postdoctoral fellows or equivalent
Investigator-Initiated Research Award:
Investigators at or above the level of Assistant Professor or equivalent
Must commit a minimum of 10% effort throughout the award
Neurofibromatosis Research Academy – Leadership Award:
Academy Director must be an established NF investigator at or above Associate Professor or equivalent
Academy Deputy Director must also be at or above Associate Professor level and affiliated with a different institution
Neurofibromatosis Research Academy – Scholar Award:
Scholars must be early-career investigators within 10 years of terminal degree or clinical fellowship
Requires an eligible Career Guide who is an established NF investigator
Synergistic Idea Award:
Investigators at or above the level of Assistant Professor or equivalent
Additional eligibility requirements may be included in the final funding opportunity announcements.
What companies and projects are likely to win?
The NFRP is seeking projects that are:
Innovative and high-impact
Clinically relevant
Focused on improving patient outcomes
Addressing one or more stated Areas of Emphasis
Advancing understanding, diagnosis or treatment of NF and schwannomatosis
Competitive applications are likely to include:
Strong scientific rationale
Significant translational potential
Collaborative or multidisciplinary approaches
Novel technologies or methodologies
Preliminary and/or published data where required
Certain award mechanisms specifically encourage:
High-risk, high-gain concepts
Multi-investigator collaboration
Data science approaches
Open science participation
Mentorship and workforce development in NF research
The solicitation also emphasizes research that could benefit Service Members, Veterans and the broader public.
Are there any restrictions I should know about?
Yes. Key restrictions include:
Clinical trials are not allowed under the listed award mechanisms
Several award mechanisms require preliminary and/or published data
All applications require a pre-application submission through eBRAP before full application submission
Multiple award mechanisms require submission of a letter of intent prior to full application submission
Applications must conform to the final funding opportunity announcements posted on Grants.gov
The pre-announcement states that investigators should not construe the notice as an obligation or promise by the government.
How long will it take me to prepare an application?
Preparation timelines will vary significantly depending on the award mechanism.
Applicants pursuing:
Multi-institutional collaborations
Academy proposals
Large-scale synergistic projects
Open science options
should expect substantially longer preparation timelines due to coordination requirements, mentoring structures, collaborator commitments and supporting documentation.
Because all applications require pre-applications and several require letters of intent, applicants should begin planning before the official funding opportunity announcements are released.
How can BW&CO help?
BW&CO can support applicants with:
Opportunity assessment and award mechanism selection
Research strategy positioning
Commercialization and impact narrative development
Proposal writing and editing
Collaboration structuring
Project management and submission coordination
Budget development support
Grants.gov and eBRAP submission support
Reviewer-style proposal feedback
Additional Resources
ARPA- E INSPIRING GENERATIONS OF NEW INNOVATORS TO IMPACTTECHNOLOGIES IN ENERGY 2026 (IGNIITE 2026)
Deadline: May 29th, 2026
Funding Award Size: $500k
Description: Apply by 9:30 AM ET, May 29, 2026 for ARPA-E IGNIITE 2026 funding. Early-career innovators can receive up to $500K for transformative energy technologies plus mentorship and national exposure.
Below is a brief summary. Please check the full solicitation before applying (link in resources section).
Executive Summary:
The IGNIITE 2026 program from ARPA-E is a high-prestige, early-career funding opportunity designed to support transformational, high-risk energy technologies. It is not founder-friendly in structure (no teams, no co-PIs), but offers meaningful non-dilutive funding and strong ecosystem access.
You must first submit a Concept Paper by 9:30 AM ET, May 29, 2026.
If selected, you may be invited to submit a full application. With only ~$10M total funding and awards capped at $500K, this is a competitive but accessible entry point into ARPA-E for early-career innovators.
How much funding would I receive?
Individual awards: up to $500,000
Potential additional funding:
Up to $250,000 Director’s Award (at ARPA-E’s discretion)
Total program funding: approximately $10 million
Number of awards: Not specified (ARPA-E may issue one, multiple, or no awards)
What could I use the funding for?
Applicants are advised to assess whether their proposed technologies are aligned with the DOE’s current areas of interest. Those areas include, but are not limited to:
Energy supply chain security (to include critical minerals)
Advanced nuclear (to include fusion, fission)
Geothermal
Grid reliability and security
American manufacturing competitiveness
Are there any additional benefits I would receive?
Yes—this program includes structured ecosystem access:
Participation in the IGNIITE Annual Program (two one-week sessions in Washington, D.C.)
Training (e.g., proposal writing, commercialization, pitching)
Direct engagement with:
ARPA-E Program Directors
Investors
Federal stakeholders
Mentorship and networking opportunities
What is the timeline to apply and when would I receive funding?
Key deadlines:
Concept Paper questions deadline: 5 PM ET, May 19, 2026
Concept Paper submission deadline: 9:30 AM ET, May 29, 2026
Invite / Not Invite notifications: 5 PM ET, July 14, 2026
Full application deadline: Not specified (TBD)
Selection notifications: September 2026 (anticipated)
Award start: December 2026 (anticipated)
Period of performance:
December 2026 – December 2028
Where does this funding come from?
Advanced Research Projects Agency—Energy (ARPA-E)
Within the U.S. Department of Energy (DOE)
Authorized under federal statute (America COMPETES Act and subsequent amendments).
Who is eligible to apply?
This program is highly specific and restrictive:
Principal Investigator (PI) requirements
Must be an early-career researcher
PhD received within 8 years of the Concept Paper deadline
Must be:
U.S. citizen, permanent resident, or green card applicant
If at a university:
Must be a pre-tenure Assistant/Associate Professor
Must self-direct the project (no co-PIs allowed)
Eligible organizations
For-profit companies
Universities
Nonprofits
DOE labs / FFRDCs
Additional constraints:
Must apply as a standalone applicant (no teams or subrecipients)
Must be U.S.-based with majority domestic ownership
What companies and projects are likely to win?
Competitive projects will:
Be transformational (not incremental)
Have potential to be disruptive in the market
Demonstrate clear technical risk with high upside
Include hypothesis-driven R&D with measurable outcomes
ARPA-E prioritizes:
Novel concepts that could create new technology “learning curves”
Technologies with clear commercialization potential
Strong technical justification and feasibility
Projects will be rejected if they:
Are incremental improvements
Lack scientific rigor
Cannot scale or become disruptive
Are there any restrictions I should know about?
Key restrictions include:
No cost share required
Must spend at least 5% on Technology Transfer & Outreach (TT&O)
Work must generally be performed in the U.S.
Limited or restricted:
Foreign participation (requires waiver)
Foreign travel
Major construction
Other constraints:
Cannot submit more than one application per PI
Must comply with strict federal reporting, disclosure, and security requirements
How long will it take me to prepare an application?
Based on requirements:
Concept Paper (required first step)
Includes:
Technical concept (4 pages)
Personal qualification summary (2 pages)
Summary slide
Letter of support
Transcript
Full Application (if invited)
Includes:
15-page technical volume
Budget workbook
Multiple federal forms and disclosures
Biosketches and support documentation
Estimated effort:
Concept Paper: 2–4 weeks
Full Application: 6–10+ weeks
How can BW&CO help?
BW&CO can support you across the full process:
Positioning your concept as “transformational” (not incremental)
Translating technical ideas into ARPA-E-aligned narratives
Structuring your Concept Paper for invite likelihood
Building a clear commercialization and impact story
Managing compliance with ARPA-E formatting and submission rules
Additional Resources
Low-Cost Uncrewed Combat Attack System (LUCAS) Component Challenge
Deadline: Rolling Deadline
Funding Award Size: $500k - $5m
Description: Apply to the LUCAS Component Challenge for funding to develop low-cost UAV components and defense technologies. Open for 120 days with rolling reviews and rapid awards.
Below is a brief summary. Please check the full solicitation before applying (link in resources section).
Executive Summary:
The Low-Cost Uncrewed Combat Attack System (LUCAS) Component Challenge is an open, rolling solicitation seeking dual-use technologies that reduce cost and improve performance across LUCAS subsystems. This is not for building a full aircraft—it is strictly for components that can integrate into existing or future LUCAS platforms.
The challenge window is open for one hundred twenty days from posting, with weekly reviews and rapid down-selects anticipated within thirty to forty-five days of submission. Companies that are ready to deliver testable prototypes quickly should apply as early as possible to maximize selection odds.
Deadline is June 24th, 2026.
How much funding would I receive?
Funding typically ranges from $500k - $5m per award.
Desired Solution
The government seeks prototypes and concepts that reduce cost, increase performance, improve manufacturability, and strengthen mission adaptability across the LUCAS family. Components may target aircraft already fielded, upcoming variants, or platform-agnostic interfaces intended for future LUCAS systems.
These technology areas include:
a) Artificial Intelligence (AI): Machine learning, perception, autonomy, and decision aids that enhance mission planning, predictive maintenance, and autonomous performance while reducing operator workload.
b) Mission Command Planner and Executor: Tools that translate commander intent into executable tasking for LUCAS platforms, enabling rapid re-tasking, synchronization, and secure mission execution.
c) Payload – Kinetic and Non-Kinetic: Modular payloads providing offensive, defensive, and sensing effects, emphasizing rapid interchangeability, safe integration, and interoperability across mission profiles.
d) Navigation Systems: Avionics and navigation suites resilient to degraded or GPSdenied environments, leveraging multi-sensor fusion, inertial navigation, and antijam/anti-spoofing technologies.
e) Alternative Energy: Onboard or distributed energy systems that extend endurance, reduce logistics burden, and enable sustained operations, including hybrid, fuel cell, or regenerative power options.
f) Engines: Power and propulsion units focused on reliability, maintainability, and energy efficiency, supporting rapid maintenance and multi-fuel adaptability.
g) Manufacturing Capabilities: Advanced production methods such as additive manufacturing and modular assembly that reduce cost, shorten lead times, and improve supply chain resilience.
h) Test and Evaluation Capabilities: Rapid, repeatable validation tools and instrumentation, including hardware-in-the-loop, automated test frameworks, and performance data analytics.
i) Integration Labs: Physical or virtual environments that accelerate interoperability testing, software-hardware integration, and government-industry co-development using standardized interfaces.
j) One-Way Attack Systems: Affordable, expendable loitering or single-use systems emphasizing safety, accuracy, and low-cost production for tactical effects.
k) Range-Extending Technologies: Communication relays, propulsion enhancements, or networked systems that expand operational reach, endurance, and mission duration. Together, these areas represent the spectrum of component and subsystem innovation needed to enhance LUCAS performance, reduce lifecycle costs, and enable scalable production across multiple mission sets.
l) Swarm & Collaborative Autonomy: Distributed sensing, mesh networking, cooperative tasking, and multi-vehicle behaviors.
m) Safety, Reliability & Self-Diagnostics: Pre-flight auto-check systems, onboard selfassessment tools, safe-to-arm mechanisms, and lightweight encryption modules.
n) Launch & Recovery Innovations: Low-cost launch systems, expeditionary recovery kits, modular or disposable launch rails, and ruggedized capture solutions.
o) Environmental Hardening & Weatherization: Corrosion protection, weatherproofing, low-temperature battery chemistry, and ruggedized housings.
Are there any additional benefits I would receive?
Yes. Selected companies may receive:
Direct collaboration with LUCAS manufacturer (Spektreworks) or integrator (Neany)
Access to government-provided interfaces, labs, and test environments (post down-select)
Opportunity for follow-on funding for testing or production
Exposure to multiple government stakeholders reviewing submissions on a rolling basis
What is the timeline to apply and when would I receive funding?
Application window: open for one hundred twenty days from posting
Submission reviews: weekly
Down-select decisions: typically within thirty to forty-five days of submission
Post-award expectation: solutions should be ready for demonstration within ninety days of award
Funding timing beyond this is not specified in the solicitation.
Where does this funding come from?
Funding is issued through:
One Nation Innovation (ONIX) Other Transaction Authority (OTA)
Operated on behalf of government partners, with coordination from OUSD R&E
Who is eligible to apply?
The challenge is broadly open to:
Small and nontraditional vendors
Startups and early-stage companies
Commercial dual-use developers
International partners (subject to regulations)
No prior DoD experience is required.
What companies and projects are likely to win?
Competitive submissions will:
Demonstrate clear cost reduction or cost-per-effect improvements
Be ready for testing within ninety days of award
Integrate easily with government systems and open interfaces
Show manufacturability, scalability, and supply chain resilience
Provide a credible delivery schedule and transition pathway
Evaluation prioritizes:
Open architecture and interoperability
Cost and total ownership impact
Technical maturity and readiness
Integration simplicity and safety
Speed to delivery
Are there any restrictions I should know about?
This challenge does not fund full LUCAS aircraft development—components only
Work is expected to be unclassified, but may involve export control or CUI compliance
CUI cannot be submitted through the platform
Vendors are responsible for regulatory compliance
Selected vendors may receive controlled government data post down-select
How long will it take me to prepare an application?
The solicitation requires:
A proposal of no more than 10 pages in 12-point Arial
A separate cover page with company and contact details
Required content includes:
Technical approach and cost reduction strategy
Integration and testing plan
Rough order of magnitude pricing
Past performance
Delivery schedule
Preparation time is not specified in the solicitation.
How can BW&CO help?
BW&CO can:
Position your component against LUCAS evaluation criteria
Translate your technology into a clear cost-reduction and integration narrative
Align your proposal with OTA expectations and rapid prototyping goals
Develop a compelling, compliant 10-page submission optimized for fast down-select
Additional Resources
Fort Stewart & Hunter Army Airfield Energy Resiliency Microgrid Prototype & Lines of Effort (LOEs) Challenge through ONIX OTA Partnership
Deadline: May 19th
Funding Award Size: $500k - $5m
Description: Apply by May 19, 2026 at 07:00 PM for U.S. Army funding to design and deploy a solar + battery microgrid at Fort Stewart. Prototype project with follow-on potential at Hunter Army Airfield.
Below is a brief summary. Please check the full solicitation before applying (link in resources section).
Executive Summary:
The USARMY – Fort Stewart & Hunter Army Airfield Energy Resiliency Microgrid Prototype is a prototype-focused opportunity to design, build, and validate a solar-plus-storage microgrid supporting mission-critical operations. The Army is seeking solutions that can demonstrate real-world resiliency performance and produce a replication package for future deployments.
Applications close May 19, 2026 at 07:00 PM.
This is a fast-moving opportunity with a 30–45 day anticipated down-select, requiring concise (2–10 page) submissions and a clear, executable approach.
How much funding would I receive?
Funding typically ranges from $500k - $5m per award.
AREAS OF INTEREST
LOE 1: Prototype / Program Management, Permitting, and Stakeholder Coordination
Provide program management and dedicated oversight to execute the Fort Stewart microgrid prototype, including end‑to‑end coordination of permitting and stakeholder actions required for successful deployment.
● Provide program management, schedule/risk governance, and coordination to execute the Fort Stewart microgrid prototype within the Government-directed timeline.
● Lead and track permitting actions for the solar farm and adjacent battery facility (BESS); coordinate documentation packages and approvals with installation stakeholders and authorities having jurisdiction, as directed.
● Maintain an integrated risk register and readiness gates for design, permitting, installation, commissioning, and testing; provide recurring status reporting and issue resolution as directed.
● Coordinate site access, safety planning, and installation coordination actions required to enable on‑site work and testing activities, as directed.
LOE 2: Prototype / Microgrid Design, Build, Integration, and Commissioning (Fort Stewart)
Execute the Fort Stewart solar-plus-storage microgrid prototype to validate installation energy resiliency under outage/degraded-grid conditions, while coordinating required permitting and stakeholder actions to enable successful deployment.
● Design and implement the solar‑plus‑storage microgrid architecture, including interconnection, controls, protection schemes, and operating modes necessary to support mission‑essential loads during outages/degraded grid conditions, as directed.
● Install, integrate, and commission the solar farm and battery energy storage system (BESS), and deliver as‑built documentation and configuration baselines for the prototype system.
● Coordinate construction/installation sequencing with Government stakeholders to support access, safety, and continuity of installation operations, as directed.
● Prepare commissioning checklists and acceptance test procedures consistent with Government-directed requirements; document results and corrective actions through closeout.
LOE 3: Prototype / Performance Validation, Sustainment Readiness, and Replication Package (HAAF)
Validate prototype performance through representative testing, deliver sustainment readiness artifacts, and provide a replication kit to accelerate sequential deployment at Hunter Army Airfield.
● Execute a Government‑approved demonstration plan that includes at least one planned utility‑outage/islanding demonstration and one degraded‑grid scenario; document results, constraints, and recommended design/process changes.
● Establish baseline resiliency performance and report measurable deltas from testing (e.g., critical load support duration, transfer time to islanded operations, system availability/uptime, recovery time), with decision‑quality evidence suitable to inform sequential deployment.
● Deliver operator/maintainer training, safety procedures, sustainment recommendations, and turnover artifacts required for continued operations, as
directed.
● Deliver a microgrid replication kit to accelerate sequential deployment at Hunter Army Airfield, including process map, permitting playbook, reference
architecture, commissioning checklist, operator training package, and lessons‑learned delta list.
● Coordinate with the Government to define the mission-essential load set and target sustainment duration for demonstration events prior to execution, as directed.
Are there any additional benefits I would receive?
Yes—non-dilutive and strategic benefits include:
Opportunity to deliver a first-of-its-kind microgrid at Fort Stewart
Positioning for follow-on deployment at Hunter Army Airfield (approximately 1+ year out)
Creation of a replicable implementation package for future Army installations
Direct engagement with the U.S. Army and ONI through an ONIX OTA contracting pathway
What is the timeline to apply and when would I receive funding?
Application deadline: May 19, 2026 at 07:00 PM
Down-select timeline: ONI anticipates 30–45 days from posting
Project duration: Approximately 1–1.5 years for Fort Stewart execution
Timing for award and funding disbursement is not specified in the solicitation.
Where does this funding come from?
U.S. Army (Fort Stewart & Hunter Army Airfield)
Contracting via ONIX OTA in coordination with ACC-RI
Who is eligible to apply?
U.S.-based industry (i.e., small businesses), academic, and nonprofit organizations
Must register and submit via https://gocolosseum.org
What companies and projects are likely to win?
Proposals will be evaluated across four weighted categories:
1. Technical Approach & Design (30%)
Strong solar + battery integration design
Clear outage/islanding capability
Robust permitting and compliance strategy
2. Execution Capability & Schedule (25%)
Realistic 1–1.5 year execution plan
Defined staffing and resource allocation
Credible cost and milestone structure
3. Deliverables & Outcomes (30%)
Demonstrable performance metrics (e.g., load support duration, uptime)
Complete replication package
Strong sustainment readiness documentation
4. Past Performance & Organization Capability (15%)
Relevant microgrid or energy resiliency experience
Experience working on military or government installations
Are there any restrictions I should know about?
This is a prototype-focused effort; recurring environmental compliance services are not intended unless explicitly directed
Submission format is flexible, but proposals must include required elements (e.g., technical approach, schedule, costs, deliverables)
Responses must be 2–10 pages maximum
How long will it take me to prepare an application?
The solicitation requires a short response (2–10 pages) including technical, cost, and execution details.
Typical preparation effort will depend on readiness, but the required components include:
Technical approach
Schedule and milestones
Cost estimate (ROM)
Past performance
Company information
How can BW&CO help?
BW&CO can support:
Translating your microgrid solution into a clear, evaluation-aligned proposal
Structuring your response to directly match the scoring rubric (technical, execution, outcomes, past performance)
Developing a credible ROM cost model and milestone plan
Positioning your team’s experience for DoD evaluators and OTA pathways
Additional Resources
AIR COMBAT COMMAND A2 & AIR FORCE INTELLIGENCE COMMUNITY (ACC/A2 & AF IC) COMMERCIAL SOLUTIONS OPENING (CSO) SOLICITATION NUMBER: FA7037-26-S-C001
Deadline: ASAP
Funding Award Size: $500k - $5m
Description: Explore the ACC/A2 & Air Force Intelligence Community CSO (FA7037-26-S-C001). Monitor for AI, cyber, JADC2, and data innovation funding opportunities.
Below is a brief summary. Please check the full solicitation before applying (link in resources section).
Executive Summary:
This is an Air Combat Command A2 & Air Force Intelligence Community (ACC/A2 & AF IC) Commercial Solutions Opening (CSO) seeking innovative commercial technologies to support intelligence, AI, cyber, and multi-domain operations.
Important: You cannot apply yet. This is an umbrella CSO with Calls, meaning proposals are only accepted when specific Calls are released. Unsolicited proposals are not accepted.
The CSO is open-ended and allows Calls to be issued indefinitely with annual updates.
How much funding would I receive?
Funding typically ranges from $500k - $5m per award.
AREAS OF INTEREST
TOPIC 001: Data, Artificial Intelligence, and Decision Dominance
AI-Driven Predictive Intelligence Analysis
AF IC seeks solutions that leverage Artificial Intelligence and Machine Learning (AI/ML) to move from a reactive to a predictive intelligence posture. Capabilities should include the autonomous analysis of multi-intelligence (multi-INT) data to anticipate adversary actions, identify emerging threats, and drastically reduce the time required to generate and disseminate tactical intelligence.
Human-Machine Teaming for Accelerated Sense-Making
To overcome information overload, AF IC seeks intuitive platforms that enable seamless collaboration between human analysts and AI agents. The Government is interested in solutions that augment human cognition, automate laborious tasks, and utilize advanced visualization to help analysts make sense of vast, complex datasets at machine speed.
Commercial Data Integration and Analysis
AF IC requires innovative methods and platforms to rapidly identify, vet, ingest, and integrate commercially available information and data streams into our intelligence workflows. This includes, but is not limited to, commercial satellite imagery, Radio Frequency (RF) sensing data, public records, and internet-of-things (IoT) data to enrich and add context to classified intelligence.
Information Operations and Counter-Disinformation
AF IC seeks solutions capable of monitoring the global information environment to detect, analyze, and track adversary propaganda and disinformation campaigns. Key capabilities include sentiment analysis, source attribution, and the generation of data-driven counternarratives to ensure information superiority.
TOPIC 002: All-Domain Command & Control
Joint All-Domain Command and Control (JADC2), Data Integration and Fusion
To realize the vision of AF IC, the JADC2 needs a robust "digital backbone" to fuse data from disparate sensors and platforms across all domains. The Government seeks solutions for a common data layer that can normalize, process, and share Intelligence, Surveillance, and Reconnaissance (ISR) data in a secure, resilient, and cloud-native environment to create a common operating picture.
Multi-Domain Operations (MDO) Battle Management
AF IC is interested in advanced battle management tools that enable the planning, 6 coordination, and synchronized execution of multi-domain operations. Solutions should provide the Government with decision-making aids to understand the cross-domain impacts of kinetic and non-kinetic effects in a dynamic environment.
Digital Twin and Engineering for Mission Rehearsal, Tactics Development, and Training
AF IC seeks to create a high-fidelity, continuously updated digital twin of the battlespace. The primary purpose of this environment is to enable the testing of tactics, rapid development and validation of new Tactics, Techniques, and Procedures (TTPs), and advanced mission rehearsal for aircrews, operators, and planners in complex, multidomain contingencies, thereby improving readiness while reducing risk.
TOPIC 003: Resilient Cyber and Intelligence, Surveillance, Reconnaissance Operations
Advanced Sensing and Data Processing at the Edge
As operations expand into contested, communication-denied environments, the Government requires solutions that enable the processing, exploitation, and dissemination (PED) of sensor data at the tactical edge. AF IC is interested in low Size, Weight, and Power (low-SWaP) hardware and software that can perform on-platform AI/ML inference to deliver time-sensitive intelligence directly to the warfighter.
Advanced Cyber Threat Intelligence
To proactively defend our networks, the Government seeks predictive analytic platforms that can identify emerging cyber threats, TTPs, and malware before they are used against government systems. Solutions should provide actionable, machine-readable threat intelligence that can be automatically ingested by government defensive cyber platforms.
Quantum-Resistant Cryptography and Secure Communications
AF IC requires a layered defense to detect, track, identify, and neutralize hostile Small Unmanned Aerial Systems (sUAS) threats. The Government is soliciting for commercial solutions for all aspects of the counter sUAS mission, including passive and active sensors, command and control integration, and kinetic and non-kinetic effectors.
Signals Intelligence (SIGINT) Modernization
AF IC seeks to modernize government SIGINT capabilities with commercial technologies that leverage software-defined radios (SDR), advanced signal processing, and AI/ML for automated signal detection, classification, and geolocation across a congested and contested electromagnetic spectrum.
Cognitive Electronic Warfare (EW)
AF IC seeks to modernize our SIGINT capabilities and develop a cognitive EW capability that leverages AI/ML for automated signal detection, classification, and geolocation. The Government is interested in software-defined systems that can autonomously sense and dynamically respond to novel threats across a congested and contested electromagnetic spectrum.
TOPIC 004: Foundational Digital Infrastructure
Multi-Cloud Abstraction, Orchestration, and FinOps for C2E
The AF IC operates in a multi-cloud environment via the Intelligence Community's Commercial Cloud Enterprise (C2E) contract. The Government seeks a common abstraction layer or Cloud Management Platform (CMP) to provide a "single pane of glass" for managing, deploying, and securing applications across multiple classified cloud providers. Key capabilities include Infrastructure-as-Code (IaC) portability, unified security governance, and a robust Financial Operations (FinOps) dashboard to optimize cloud spending across the enterprise.
TOPIC 005: Enterprise Wide Integration and Architecture Modernization
The ACC/A2 seeks innovative solutions to support the integration of data across disparate monitoring phenomenologies and modernization of hardware/software architectures. This topic includes:
New solutions to integrate data access and discoverability across varying monitoring phenomenologies to lower detection thresholds and/or increase efficiency of current operations.
Technologies to modernize hardware/software architectures or implement improved software design and accrediting processes to more flexibly meet mission needs.
TOPIC 006: Enterprise Asset and Lifecycle Management Improvements
The ACC/A2 seeks innovative solutions that can provide enterprise-wide asset management visibility as well as improve our lifecycle management capabilities. This topic includes:
Increase accuracy of forecasting of requirements and scheduling of procurements through the use and exploitation of supply chain demand data
Supply chain management, specifically: Automated systems to reduce/eliminate inefficiency, improve asset control, decrease touchpoints and minimize inventory
Automated identification and reporting of components and systems with substandard reliability
Are there any additional benefits I would receive?
The CSO states potential for:
Contracts or Other Transaction Agreements (OTAs)
Follow-on increases in award value and scope as solutions mature
What is the timeline to apply and when would I receive funding?
A deadline is to be released in the coming days. We’re planning to assist companies with meeting appropriate personnel and are beginning that work promptly.
Where does this funding come from?
Air Combat Command A2 (ACC/A2)
Air Force Intelligence Community (AF IC)
Authorized under:
10 U.S.C. 3458
R-DFARS 212.70
Who is eligible to apply?
For Step Two (full proposal), offerors must:
Be registered in SAM.gov
Be considered responsible under federal regulations
Have a satisfactory performance record
Be eligible under federal law
The solicitation references:
Small businesses
Nontraditional defense contractors (as defined in 10 U.S.C. § 2302(9))
What companies and projects are likely to win?
Based on the solicitation, competitive solutions will:
Be innovative (new or new application of existing tech)
Be commercial or commercializable
Align directly with AF IC mission needs
Be built for:
Cloud-native environments
AI-enabled workflows
Secure, scalable deployment
Strong proposals will also demonstrate:
Integration with Zero Trust and ICAM
Compatibility with DevSecOps and continuous ATO (cATO)
Use of open architectures (SOSA / OMS)
Are there any restrictions I should know about?
Yes:
Unsolicited proposals will not be accepted
Do not submit proprietary, classified, or sensitive information in responses
Must comply with:
Cybersecurity requirements (CMMC levels per Call)
SAM registration and UEI requirements
Other constraints:
Government may award all, part, or none
Government is not obligated to make any award
Offerors bear all proposal preparation costs
How long will it take me to prepare an application?
The structure implies:
White Paper (2–5 pages) + Quad Chart for Step One
Full proposal only if invited
Actual timelines will be defined in each Call.
How can BW&CO help?
BW&CO can support you to:
Monitor and identify relevant Calls as soon as they are released
Shape your solution to align with:
AF IC priority topics
Zero Trust, DevSecOps, and open architecture requirements
Develop:
High-impact white papers and quad charts
Full proposals for Step Two
Position your company as a credible commercial partner to DoD/IC buyers
Additional Resources
Defense Industrial Base Consortium (DIBC) -Industrial Base Analysis and Sustainment (IBAS) - RFP 26-01
Deadline: ASAP
Funding Award Size: Up to $8.3M
Description: Apply for DIBC IBAS funding to scale domestic manufacturing and secure supply chains. Up to $8.3M available for prototype projects in microelectronics, rare earth magnets, forging, and RF systems. Deadline not specified.
Below is a brief summary. Please check the full solicitation before applying (link in resources section).
Executive Summary:
The Defense Industrial Base Consortium (DIBC) is soliciting prototype solutions to address critical domestic supply chain vulnerabilities and manufacturing capability gaps across four priority areas. These efforts are funded under the Industrial Base Analysis and Sustainment (IBAS) program using RDT&E appropriations and are tied to Congressional Interest.
Companies should move quickly if aligned—this is a targeted, single-award-per-topic opportunity with defined funding ceilings and strong Government interest in scaling domestic capacity.
How much funding would I receive?
Funding is structured as single awards per topic, each capped at the following levels:
Topic 1: Secure Processor Development — Up to $8,300,000 (RDT&E)
Topic 2: Rare Earth Magnet Manufacturing — Up to $2,500,000 (RDT&E)
Topic 3: Industrial Forge Quenching Capacity Improvement — Up to $2,500,000 (RDT&E)
Topic 4: RF Contested Environments — Up to $4,400,000 (RDT&E)
The Government intends to make one award per topic, not exceeding the stated funding limitation.
RESEARCH TOPICS:
-
The Government requires a prototype project to develop, mature, and scale the domestic production of advanced secure processors for defense applications. Modern defense systems operating at the tactical edge require high-performance computing (eg, AI/ML processing, sensor fusion) while maintaining an absolute Zero-Trust hardware posture. Current commercial-off-the-shelf (COTS) processors are vulnerable to supply chain interdiction, side-channel attacks, and reverse engineering.
Technical Focus: Solutions should emphasize hardware roots of trust (RoS), secure boot mechanisms, inline memory encryption, and resistance to physical and electrical side-channel attacks. Proposals may include advanced 2.5D and 3D heterogeneous integration (HI) packaging, or the integration of secure processor chiplets (such as RISC-V architectures with integrated memory guards) into larger systems on a chip (SoC).
Funding Limitation: Up to $8,300,000 (RDT&E). The Government intends to make a single award no greater than the funding limitation. Teaming arrangements are acceptable and encouraged to meet complex supply chain requirements.
-
The Government requires prototype solutions to establish or enhance domestic manufacturing capabilities for high-performance rare earth permanent magnets, specifically Neodymium-Iron-Boron (NdFeB) and Samarium-Cobalt (SmCo). These magnets are critical for defense electric drive systems, radar, missile guidance fins, and advanced actuators (e.g., F-35 and submarine platforms). Currently, foreign entities of concern control over 85% of the global magnet processing and production capacity.
Technical Focus: The project must advance a verifiable, secure "mine-to-magnet" supply chain completely bypassing foreign entities of concern. The project may use virgin material sources or recycled materials. Technical approaches should highlight advanced sintered manufacturing processes, heavy rare earth (HRE) separation capabilities (specifically isolating Dysprosium and Terbium), or the use of Grain Boundary Diffusion (GBD) technology to maximize high-temperature performance while reducing overall reliance on scarce HREs.
Funding Limitation: Up to $2,500,000 (RDT&E). The Government intends to make a single award no greater than the funding limitation. Teaming arrangements are acceptable and encouraged to meet complex supply chain requirements.
Economic Participation: To ensure a resilient domestic supply chain, the Government seeks solutions demonstrating shared financial investment and long-term commercial sustainment. In alignment with the IBAS mission to establish and diversify regional centers of excellence, the Government will favorably evaluate proposals that build or utilize robust industrial infrastructure, integrate localized supply chains, and develop specialized workforces for domestic magnet manufacturing. The highest evaluation preference will be given to proposed solutions that strategically locate operations within established or rapidly emerging U.S. automotive, aerospace, or advanced manufacturing corridors to leverage existing industrial synergies."
-
Heavy forging is a foundational requirement for major defense platforms, particularly within the Submarine Industrial Base (SIB), shipbuilding, and heavy armor. The Government requires a prototype project to design, upgrade, and validate improved industrial forge quenching capacity. Current domestic infrastructure is a major bottleneck, leading to extended lead times for ultra-large cast and forged components.
Technical Focus: Solutions must demonstrate the implementation of advanced quenching infrastructure (eg, large-scale water, oil, or polymer quench tanks). The technical approach should feature automated, sensor-driven temperature monitoring and controlled cooling rates to guarantee metallurgical consistency, prevent stress fractures in heavy steel/titanium alloys, and significantly increase throughput for Navy and Army platform components.
Funding Limitation: Up to $2,500,000 (RDT&E). The Government intends to make a single award no greater than the funding limitation. Teaming arrangements are acceptable and encouraged to meet complex supply chain requirements.
Economic Participation: To meet the IBAS strategic requirement for expanding geographically distinct heavy industrial infrastructure, the Government seeks proposals that drive direct economic participation and localized industrial impact. The highest evaluation preference will be given to proposed solutions that establish or expand operations within regions offering established heavy manufacturing ecosystems, high-capacity energy grids, and strategic logistical access to rapidly scale domestic infrastructure capabilities."
-
The Department of War (DoW) requires domestic, trusted prototyping and low-rate initial production of advanced microelectronics capable of maintaining spectrum dominance in severely contested and congested electromagnetic environments.
Currently, the U.S. Defense Industrial Base (DIB) faces a critical gap in fielding ultra-wideband, low-latency RF signal processing components at the tactical edge. Near-peer adversaries have proliferated sophisticated Electronic Warfare (EW) systems designed to jam, spoof, or degrade DoW communications, radar, and precision-guided munitions. Existing silicon-based microelectronics lack the instantaneous bandwidth and dynamic range required to filter intentional interference and isolate signals of interest in real-time, posing a severe risk to Joint All-Domain Command and Control (JADC2) survivability.
· Technical Focus: The solution must be centered on the design, development, and prototyping of advanced microelectronic architectures capable of maintaining spectrum dominance in highly contested and congested Radio Frequency (RF) environments. To counter sophisticated near-peer Electronic Warfare (EW) and jamming capabilities, the proposed solution must deliver ultra-wideband signal processing beyond the state of the practice at the tactical edge. This requires moving beyond traditional narrowband, high-latency digital conversion by integrating analog, mixed-signal, or photonic pre-processing directly on-chip. These advanced microelectronic components must demonstrate the high dynamic range necessary to simultaneously nullify high-power, frequency-hopping interference while isolating and preserving critical, low-power signals of interest in real-time without introducing processing lag.
Furthermore, the technical focus mandates strict adherence to Size, Weight, Power, and Cost (SWaP-C) optimization to ensure the resulting prototypes are viable for integration into constrained platforms such as Unmanned Aerial Systems (UAS), precision-guided munitions, and mobile Joint All-Domain Command and Control (JADC2) nodes. A critical execution requirement of this effort is the active utilization and maturation of the domestic supply chain, specifically leveraging the established optics, photonics, and RF microelectronics industrial base. Performers must explicitly demonstrate how their technical approach integrates specialized manufacturing, advanced prototyping, and research capabilities to deliver military-grade, environmentally hardened sub-systems (targeting Technology Readiness Level 5 or 6) that are ready for transition into Department of War (DoW) Programs of Record.
Funding Limitation: Up to $4,400,000 (RDT&E). The Government intends to make a single award no greater than the funding limitation. Teaming arrangements are acceptable and encouraged to meet complex supply chain requirements.
Are there any additional benefits I would receive?
This program is structured around Government equity, meaning participation may include:
Government Purpose Rights (GPR) to technical data and software
Priority access or reserved production capacity
Delivery of prototypes, tooling, or LRIP units
Shared licensing or royalty-free use of developed IP
Additionally, projects are tied to Congressional Interest and may position companies for future defense production and transition opportunities.
What is the timeline to apply and when would I receive funding?
A deadline is to be released in the coming days. We’re planning to assist companies with meeting appropriate personnel and are beginning that work promptly.
Where does this funding come from?
Funding comes from:
Research, Development, Test, and Evaluation (RDT&E) appropriations
Managed under the Industrial Base Analysis and Sustainment (IBAS) program
Executed through the Defense Industrial Base Consortium (DIBC)
These efforts are explicitly tied to national security priorities and Congressional Interest.
Who is eligible to apply?
Members of the Defense Industrial Base Consortium (DIBC) may submit solution papers
Teaming arrangements are acceptable and encouraged
No additional eligibility criteria are specified in the solicitation.
What companies and projects are likely to win?
Competitive proposals will:
Directly address critical supply chain vulnerabilities
Demonstrate ability to scale domestic manufacturing capacity
Align tightly with IBAS objectives
Show regional industrial impact and infrastructure development
Include shared financial investment and long-term sustainment plans (where applicable)
Leverage or build localized supply chains and workforce development
Highest preference is given to projects that:
Strengthen regional industrial hubs
Integrate into existing U.S. automotive, aerospace, or manufacturing corridors
Reduce reliance on foreign entities of concern
All topics are evaluated independently.
Are there any restrictions I should know about?
Key requirements and constraints include:
The Government expects equity commensurate with its investment
Projects must align with IBAS statutory objectives
Solutions must support domestic supply chain resilience
Certain topics require fully domestic supply chains bypassing foreign entities of concern
Deliverables may include data rights, IP access, and production commitments
Additional topic-specific technical constraints apply (e.g., SWaP-C requirements, secure architectures, metallurgical controls).
How long will it take me to prepare an application?
Not specified in the solicitation.
How can BW&CO help?
BW&CO can support:
Opportunity qualification and topic alignment strategy
Structuring competitive Solution Papers
Positioning your project for IBAS evaluation criteria
Building teaming strategies and supply chain narratives
Translating technical concepts into clear, fundable proposals
Additional Resources
U.S. DOT SBIR Fiscal Year 2026 (FY26) Phase I
Deadline: July 7, 2026
Funding Award Size: $200k
Description: The U.S. DOT SBIR FY26 Phase I pre-solicitation is open through May 29, 2026 at 5:00 p.m. ET. Explore key dates, funding opportunities, and how to prepare for the upcoming solicitation.
Below is a brief summary. Please check the full solicitation before applying (link in resources section).
Executive Summary:
The U.S. DOT SBIR FY26 Phase I Pre-Solicitation is now open and represents an early opportunity to align with upcoming federal R&D funding across transportation, AI, safety, and infrastructure.
The pre-solicitation is open through May 29, 2026, at 5:00 p.m. ET, which is the key near-term deadline to engage, ask questions, and position your solution.
While this is not the formal application window, companies that act now—by refining their concept, engaging in Q&A, and aligning to specific topics—will be significantly better positioned for the estimated solicitation period: June 3, 2026 – July 7, 2026.
How much funding would I receive?
Phase I funding is up to $200,000 for 6 months.
RESEARCH TOPICS:
-
This topic seeks an integrated system combining AI, edge/cloud computing, and V2X communication to detect, predict, and mitigate traffic congestion in real time across multiple intersections or regions. The solution should ingest diverse traffic data, generate location-specific operational guidance (e.g., speed, lane changes, detours), and securely deliver it to vehicles, infrastructure, and agencies. A key focus is on balancing workloads between edge and cloud systems while ensuring low latency, scalability, and secure communications.
-
FHWA is looking for a vehicle-mounted, multi-sensor inspection system that can assess catch-basin conditions (e.g., water, sediment, debris) without removing grates or requiring manual inspection. The system should use sensors (optical, lidar, radar, etc.) and AI to interpret basin conditions while in motion, improving safety and efficiency for DOTs managing large, distributed infrastructure networks.
-
This topic calls for a mobile system capable of safely discharging high-voltage lithium-ion battery systems (BESS) in rail vehicles after accidents or during maintenance. The system must handle at least 400 kW of stored energy, include robust safety features, and be operable by trained personnel. It should support multiple discharge methods (resistive, regenerative, or hybrid) and integrate with emergency response and rail maintenance workflows.
-
FTA seeks an AI-powered trip planning tool that supports the entire “Complete Trip,” from deciding to use transit through navigation and adaptation during travel. The system should integrate multimodal transportation data, personalize recommendations based on user preferences, and ensure accessibility for all users, including those with disabilities. The goal is to make transit a seamless, intuitive option compared to other modes.
-
This topic focuses on developing predictive analytics tools that use AI and integrated data sources to proactively identify safety risks in commercial transportation. A core component is a “Trusted Intermediary” framework that securely combines private industry data with public datasets while preserving privacy. The system should generate actionable, explainable insights to improve safety outcomes and resource allocation.
-
This topic seeks an AI-enabled system that predicts freight bottlenecks and supply chain disruptions using multimodal data, edge analytics, and federated learning. The solution should provide real-time insights and decision-support tools for public and private stakeholders, including dashboards and alerts. It aims to improve corridor efficiency, resilience, and coordination across transportation systems.
-
PHMSA is looking for a safe, fast, and cost-effective method to remove residual energy from end-of-life lithium-ion batteries, reducing explosion risk during transport. The solution should enable safer shipping and improve the economics of recovering critical minerals, with potential to support regulatory changes and broader commercialization.
-
This topic seeks a thermochromic coating for hazardous materials packaging that visibly changes color when internal temperatures reach dangerous levels. The coating should be durable, low-cost, and compatible with various packaging materials, providing first responders and operators with a clear, intuitive warning signal during transport or emergencies.
-
PHMSA is interested in self-repairing materials or coatings that can automatically fix damage (e.g., cracks, corrosion, punctures) in hazardous materials packaging. The solution must meet existing regulatory standards and improve safety, durability, and cost-effectiveness across bulk and non-bulk packaging applications.
-
This topic calls for a low-cost, easy-to-deploy solution to suppress lithium-ion battery fires quickly and prevent reignition. The system should work across different battery types and scenarios, integrate with emergency response workflows, and be scalable for widespread use by first responders, shippers, and operators.
Are there any additional benefits I would receive?
Not explicitly specified, but the document indicates:
Opportunities to work with federal agencies and transportation operators
Potential pilot deployments with state/local partners
Path to Phase II funding for prototype development and validation
Early positioning in priority areas like AI, safety, and infrastructure modernization
What is the timeline to apply and when would I receive funding?
Key dates provided:
Pre-solicitation open through May 29, 2026, at 5:00 p.m. ET
Pre-solicitation Q&A period: April 29, 2026 – May 29, 2026 at 5:00 p.m. ET
Estimated solicitation period: June 3, 2026 – July 7, 2026
Funding timing after submission is not specified in the provided materials.
Where does this funding come from?
Funding comes from the U.S. Department of Transportation (U.S. DOT) SBIR program, including:
Federal Highway Administration (FHWA)
Federal Railroad Administration (FRA)
Federal Transit Administration (FTA)
Office of the Secretary (OST)
Pipeline and Hazardous Materials Safety Administration (PHMSA)
Who is eligible to apply?
For-profit small businesses
What companies and projects are likely to win?
Based on the topic descriptions:
Companies building real, testable systems (not just concepts)
Teams that integrate:
AI + real-world data
Hardware + software systems
Existing infrastructure (e.g., V2X, sensors, rail systems)
Proposals that demonstrate:
Clear Phase I feasibility approach
Path to Phase II deployment
Partnerships with agencies or industry stakeholders
Solutions that address:
Safety, reliability, and scalability
Real-world operating constraints (latency, environment, compliance)
Human usability and adoption
Are there any restrictions I should know about?
Examples from the topics include:
Must integrate with existing infrastructure and systems
Must meet safety, regulatory, and operational requirements
Some topics require industry partnerships (e.g., rail stakeholders)
Certain exclusions apply (e.g., radioactive materials excluded in PHMSA 26-PH3)
Solutions must be practical, scalable, and deployable
How long will it take me to prepare an application?
Given the timeline:
You effectively have until July 7, 2026 (estimated) to prepare for submission once the solicitation opens
Early preparation during the pre-solicitation period (through May 29, 2026, at 5:00 p.m. ET) is strongly implied
How can BW&CO help?
BW&CO can help you:
Select the right topic across FHWA, FRA, FTA, OST, and PHMSA
Translate your product into a Phase I-ready technical concept
Build a clear commercialization and Phase II pathway
Develop a competitive SBIR proposal aligned to DOT expectations
Use the pre-solicitation window to refine positioning and de-risk your application
Additional Resources
Department of Education - SBIR/STTR Opportunities (IA, IB, and DT2)
Deadline: June 29th
Funding Award Size: $250k - $1m
Description: ED/IES SBIR Phase IA, Phase IB, and Direct to Phase II. Learn funding amounts, eligibility, and which track is right for your edtech startup. Deadlines June 29, 2026.
Below is a brief summary. Please check the full solicitation before applying (link in resources section).
Executive Summary:
The U.S. Department of Education (ED), through the Institute of Education Sciences (IES), is offering three SBIR funding tracks in 2026: Phase IA, Phase IB, and Direct to Phase II. These programs fund education technology companies at different stages—from early prototype to full-scale commercialization.
Phase IA: Build a brand-new product (early-stage)
Phase IB: Improve an existing product (mid-stage)
Direct to Phase II: Scale a proven innovation (late-stage)
All three tracks are competitive and mutually exclusive (you cannot submit the same or similar proposal across tracks).
Application deadline: June 29, 2026 at 11:00 a.m. Eastern Time (ET) for Phase IA and IB, and June 29, 2026 at 2:00 p.m. Eastern Time (ET) for Direct to Phase II.
How much funding would I receive?
Phase IA: $250,000 for 9 months
Phase IB: $250,000 for 9 months
Direct to Phase II: $1,000,000 for 2 years
What could I use the funding for?
Across all three tracks, funding supports:
Research and development (R&D)
Product development
Pilot testing with users
Data collection and analysis
Personnel and subcontractors
Key differences:
Phase IA: Build a new prototype from scratch
Phase IB: Develop a new component integrated into an existing product
Direct to Phase II:Scale and commercialize an existing evidence-based innovation
Are there any additional benefits I would receive?
Phase IA and IB awardees can apply for $1,000,000 Phase II funding the following year
All tracks provide federal validation and commercialization support
Direct to Phase II provides immediate access to $1M scale funding without Phase I
What is the timeline to apply and when would I receive funding?
Application timeline:
White Papers per Program: Continuous, after the posting of Q&As (Preferred)
Full proposals: By invitation only
Process:
Submit White Paper
Government evaluates for viability
If selected → invited to submit full proposal
If selected → negotiation → award
Award timing:
Not specified in the solicitation.
Where does this funding come from?
U.S. Department of Education (ED)
Institute of Education Sciences (IES)
Small Business Innovation Research (SBIR) Program
Who is eligible to apply?
For-profit small businesses
Track-specific requirements:
Phase IA: Little or no prior product development
Phase IB: Must have an existing functioning prototype or product
Direct to Phase II: Must work with an existing evidence-based innovation developed by a university or nonprofit and include the original researcher on the team
What companies and projects are likely to win?
Phase IA: Novel, high-risk ideas with strong potential impact
Phase IB: Companies with working products and a clear, innovative upgrade
Direct to Phase II: Teams with strong research evidence and a credible plan to scale
Across all tracks:
Clear problem-solution fit
Strong research and technical approach
Path to commercialization
Are there any restrictions I should know about?
Cannot submit the same or similar proposal across Phase IA, IB, or Direct to Phase II
Phase IA: Must be a new, independent product
Phase IB: New component must be distinct and not a continuation
Direct to Phase II:
Innovation must be originally developed by academic or nonprofit researchers
Cannot already be widely deployed at scale
How long will it take me to prepare an application?
Phase IA / IB: Typically 4–8 weeks
Direct to Phase II: Typically 6–10+ weeks
How can BW&CO help?
BW&CO can support:
Identify the right track (IA vs IB vs Direct to Phase II)
Position your company and product for competitiveness
Develop full technical, research, and commercialization narratives
Build compliant budgets and submission packages
Additional Resources
The National Institutes of Health Small Business Innovation Research Program
Deadline: Est. April 5, 2026; September 5, 2026
Funding Award Size: <$2.1 Million
Description: Funding for research and development toward a commercially viable product or service aligned with the missions of NIH, CDC, or FDA.
Executive Summary:
The NIH, CDC, and FDA are jointly awarding up to $2.1 million per company through the SBIR Program to support U.S. small businesses developing innovative health, biomedical, and life science technologies. Companies can apply for Phase I (proof-of-concept), Phase II (R&D and commercialization), or Fast-Track awards. Applications are due on January 5th, April 5th, and September 5th each year, with funding typically beginning 9 months after submission. Companies should begin preparing applications at least 12 weeks before a due date to complete registrations and submission.
How much funding would I receive?
Awards provide up to $323,090 for Phase I projects (up to 2 years) and $2,153,927 for Phase II projects (up to 3 years). Some topics approved by NIH may exceed these limits. Fast-Track and Phase IIB (follow-on) options allow continuous or extended funding beyond Phase II.
What could I use the funding for?
Funds may support research and development toward a commercially viable product or service aligned with the missions of NIH, CDC, or FDA (see below). Eligible costs include personnel, materials, prototypes, testing, IP protection, and other R&D expenses. Phase II and IIB funds may also be used for scale-up, validation, regulatory preparation, and commercialization efforts. Click below to see the various areas of interest:
-
NCATS supports research including, but not limited to, clinical technology, instruments, devices, and related methodologies that may have broad application to clinical research and better patient care. Our interests are in four main categories
(1) Preclinical Drug Discovery and Development
(2) Biomedical, Clinical and Health Research Informatics
(3) Clinical, Dissemination and Implementation Research
(4) Rare Diseases and Unmet Needs.
-
The NCCIH will support applications on the development of technologies and therapies relevant to complementary and integrative approaches.
Complementary health approaches include a broad range of practices and interventions that can be classified by their primary therapeutic input, including:
nutritional and natural products (e.g., special diets, dietary supplements, botanicals, probiotics, and microbial-based therapies),
psychological (e.g., meditation, hypnosis, music-based interventions, relaxation therapies),
physical (e.g., acupuncture, massage, chiropractic manipulation, other force-based manipulations, or devices related to these approaches), or
a combination of psychological and physical (e.g., yoga, tai chi, or some forms of art therapies, such as music-based interventions) input.
Additionally, NCCIH will support applications that explore the impact of complementary and integrative health approaches on health promotion, resilience, and whole person health.
Overall, NCCIH will support applications that include complementary and integrative health approaches, including multicomponent interventions that combine two or more complementary and integrative health approaches, or one or more complementary approaches integrated with one or more conventional care interventions.
-
NCI supports the Small Business Innovation Research (SBIR) and Small Business Technology Transfer (STTR) programs by engaging domestic small business concerns in federal cancer research and development that has the potential for commercialization.
-
NEI supports research including, but not limited to, the following:
Commercializable research and clinical innovations in ophthalmology and vision sciences
Commercializable therapeutics including drugs, biologics, devices, or combination therapeutics that prevent or reduce blindness or improve ocular health
Market-ready technologies and diagnostic tools for predicting, identifying, or monitoring eye diseases and vision-related conditions
Commercializable devices and services that assist people with blindness or visual impairments to improve quality of life Commercial-grade devices and support services that help individuals with blindness or vision impairments to improve and enhance their daily living experience
Market-ready technologies that correct, enhance, or augment human vision
-
Interest Areas:
Significant innovations in genomic methods or technology development. This includes, but is not limited to, advancements in nucleic acid sequencing, synthetic nucleic acid synthesis, functional genomics, single cell genomic analysis, transcriptomics, multi-omics, instrumentation, or molecular kits.
Tools and techniques that use genomics to improve patient health, such as approaches to incorporate genomic results into electronic medical records, clinical decision support tools, or genomic directed health care.
Strategies to enhance ethical, legal, and social aspects of genomics research or translation of genomics into health care.
Bioinformatics software or platforms for genomic, genetic, or sequence data processing or analysis, functional genomics, associations between genomic data and diseases or phenotypes, interpretation of variants, or genomic data integration into clinical decision making.
Databases and data management platforms for genomics research and application including platforms for sequence, functional, or phenotypic data or annotation of variants.
Development and application of methods for machine learning, pattern detection, or knowledge networks for genomics science or translation into health care.
Informatics methods and platforms that adopt data standards, enhance data sharing with privacy, and improve data exchange in genomics science or translation of genomics into health care.
Use of cloud and other computing models to improve scale, reproducibility, interoperability, cost-effectiveness, and utility of genomic and clinical data in genomics or translation into health care.
Development of curriculum and educational opportunities that increase the genomics knowledge of participants at the undergraduate, postbaccalaureate, graduate, postdoctoral, or professional levels.
-
Interest Areas:
The National Heart Lung and Blood Institute (NHLBI) is interested in supporting the development of novel therapeutics, devices, diagnostics, digital health technologies, research tools, and other innovative solutions for advancing the prevention, diagnosis, and treatment of heart, lung, blood, and sleep (HLBS) diseases and disorders.
Topics of particular interest for the NHLBI SBIR/STTR program include, but are not limited to, the following topics:
Technologies addressing HLBS complications relevant to maternal health and women’s health
Artificial Intelligence/Machine Learning technologies to improve the diagnosis, treatment, and prevention of HLBS diseases and disorders
Precision medicine approaches to treating HLBS diseases and disorders
New approach methodologies, tools, and point-of-care technologies to improve detection and therapeutic development for HLBS diseases and disorders
-
The NIA is interested in proposals to develop and validate technologies that enhance the health and wellbeing of older adults. Areas of high interest include technologies intended to address unmet needs and have clear competitive advantages, development of commercialized solutions that are cost-effective and widely available, and small businesses that are new to SBIR/STTR funding.
Scientific areas of interest include but are not limited to:
Alzheimer's Disease (AD), AD-Related Dementias (ADRD), and Age-Related Cognitive Decline:
Development of innovative tools, technologies, and interventions to prevent, diagnose, treat, monitor, or slow progression of AD/ADRD, cognitive decline, age-related sleep disorders, and delirium, including:
Biomarkers, research tools, diagnostics, imaging technologies, and AI/ML methods for early detection and monitoring.
Treatments, including cell and gene therapies, exosome-based therapeutics, behavioral and digital interventions as well as other novel approaches.
Aging Biology and Age-Related Diseases:
Development of technologies, therapeutics, biomarkers, and tools to measure, prevent, treat, or slow progression of age-related biobehavioral decline and conditions, including:
Therapeutics targeting aging biology mechanisms and personalized medicine approaches.
Research tools and data science technologies to understand aging and predict health outcomes.
Aging in Place of Choice and Care Delivery:
Development of technologies and interventions that promote healthy aging, support aging in place of choice, improve care delivery, or reduce caregiving burden, including:
Assistive devices, robotics, sensors, digital health products, and technologies to enhance care.
-
Interest Areas:
NIAAA-specific SBIR and STTR interests are tailored toward commercializing technologies that address the unique physiological, social, and clinical challenges of alcohol misuse.
The NIAAA specifically encourages small business applications in the following high-priority areas:
Biosensors and Wearables: Developing non-invasive, wearable devices for real-time alcohol monitoring (e.g., transdermal sensors) that provide more accurate data than self-reporting for research and clinical use.
Digital Health and Telehealth: Creating mobile applications, AI-driven platforms, and software for the remote delivery of evidence-based treatments, such as Cognitive Behavioral Therapy (CBT) or recovery support services.
Pharmacotherapy Development: Advancing the discovery and testing of new medications to treat Alcohol Use Disorder (AUD), specifically focusing on those with commercial potential and lower side-effect profiles.
Diagnostic Tools and Biomarkers: Innovating point-of-care diagnostic tests and biological markers for early detection of alcohol-induced organ damage (liver, brain, heart) and Fetal Alcohol Spectrum Disorders (FASD).
Advanced Data Analytics: Utilizing machine learning and big data tools to analyze large health datasets to predict relapse, identify high-risk drinking patterns, or personalize treatment plans.
Regulatory Support: Utilizing the Commercialization Readiness Pilot (CRP) to fund late-stage R&D, such as IND-enabling studies, manufacturing scale-up, or clinical trial verification required for FDA clearance.
Behavioral Interventions: Developing tools designed to improve treatment adherence, reduce stigma, or provide prevention and therapies to treat alcohol use disorder
-
Interest Areas:
The NIAID Small Business portfolio supports product development and commercialization in the areas of:
The immune system, microbe biology, and host-microbe interactions,
Diagnostic and prevention strategies
Treatment and cure strategies
-
Interest Areas:
The NIAMS small business program supports research and development of products and services for prevention, diagnosis and treatment of rheumatic, musculoskeletal and skin diseases. The research topics include, but are not limited to, the following:
Rheumatic Diseases. The NIAMS supports research on rheumatic and related diseases including rheumatoid arthritis (RA), juvenile idiopathic arthritis (JIA), Lyme arthritis, viral arthritis, gout, calcium pyrophosphate deposition disease (CPDD), spondyloarthropathies, and systemic autoimmune diseases such as systemic lupus erythematosus (SLE), systemic scleroderma (SSc), and autoimmune myositis.
Musculoskeletal Diseases. The musculoskeletal system is composed of the skeleton, the muscles, and connective tissues such as cartilage, tendon, and ligament. The NIAMS supports research aimed at improving the diagnosis, treatment, and prevention of diseases and injuries of the musculoskeletal system and its component tissues. The topics in this area include research on musculoskeletal diseases such as osteoporosis, osteoarthritis, muscular dystrophy, and osteogenesis imperfecta; tissue engineered products; orthopedic devices and implants; and sports medicine and fitness.
Skin Diseases. The NIAMS supports research on chronic inflammatory skin diseases such as psoriasis, rosacea, acne vulgaris, atopic dermatitis; autoimmune skin diseases such as pemphigus, vitiligo, and alopecia areata; skin repair and regeneration in treatment of chronic wounds and reducing scar formation; and skin cancer prevention such as products preventing skin cancer in early-stage development.
-
Interest Areas:
The NIBIB Small Business Program aims to translate cutting edge technologies into commercial products to address critical healthcare challenges. Through grants and contracts, the program supports the development of innovative biomedical technologies that improve human health. Areas of interest span biomedical imaging, medical devices, health informatics, diagnostic and therapeutic technologies, and related innovations at the intersection of biology and engineering. Projects should demonstrate strong commercial potential while addressing significant unmet clinical needs in biomedical imaging and bioengineering.
Specific program guidance includes:
Technologies may be demonstrated using a specific indication or model system, but the core innovation must be broadly applicable without significant reengineering.
Applications fall outside NIBIB's mission if the primary focus is
developing technologies to elucidate basic biological functions or disease mechanisms, or
applying and testing previously developed tools or technologies.
Per NOT-EB-21-005, NIBIB only supports early-stage clinical trials, i.e., feasibility, Phase I, first-in-human, safety, or other small clinical trials, that inform technology development. NIBIB will not support applications with efficacy, effectiveness, or a post-market concern as an outcome.
NIBIB may modify or decline funding applications for budgetary, administrative, or programmatic reasons. This includes reducing budgets, shortening award periods, or choosing not to fund applications.
Awardees are strongly encouraged to contact NIBIB's Small Business Team about the Concept to Clinic: Commercializing Innovation (C3i) Program, a mentored, entrepreneurial training course that provides innovators with essential business tools to assess the commercial viability and potential business opportunity for their product.
-
Interest Areas:
NICHD supports research that includes, but not limited to the following:
Reproductive health, including fertility, conception, contraception, and pregnancy
Health of women before, during, and after pregnancy, and fetal development and infant survival
Typical and atypical development and growth in children and adolescents, including experiences of trauma and critical illness
Gynecologic health and disease; safe and effective therapeutics and devices for children and pregnant and lactating women; dynamics of human populations across the lifespan
Optimizing function in people with intellectual, developmental, and physical disabilities
-
Interest Areas:
Consistent with NIH and Presidential priorities, the NIDA Small Business Program supports research and development of innovative medical and non-medical products and services for substance use disorders (SUDs) and adverse health consequences related to non-disordered drug use. Proposed solutions should improve access, affordability, and coordinated care across prevention, diagnosis, treatment, and recovery. NIDA prioritizes scalable solutions deployable within integrated delivery networks across healthcare, criminal justice, workforce, education, housing, and social service systems. Specific areas include, but are not limited to:
Novel, mechanism-based treatments addressing the evolving overdose crisis (e.g., synthetic opioids, stimulants, polysubstance use)
Best-in-class opioid use disorder treatments that improve retention and outcomes for individuals not adequately served by existing medications
Innovative smoking cessation therapies that enhance adherence and long-term effectiveness
First-in-class pharmacotherapeutics and medical devices for stimulant and cannabis use disorders
Diagnostic tools for detection and quantification of drug exposure
Medical devices, including digital diagnostics and therapeutics, and clinical decision support systems supporting SUDs and comorbid mental health conditions, with particular attention to pediatric populations.
Digital health technologies addressing health-related social needs
Human-biology-based new approach methodologies and other commercial research tools
Forensic testing technologies identifying emerging drugs
FDA Drug Development Tools and Medical Device Development Tools
NIDA strongly encourages applications that include early FDA engagement, consideration of regulatory pathways, payer engagement strategies, real-world evidence generation, and plans for sustainable adoption within integrated delivery networks and value-based care models.
-
Interest Areas:
NIDCD supports research including, but not limited to, the following:
Novel technologies for studying, diagnosing, and treating hearing loss, tinnitus, or balance disorders.
Novel diagnostic tools for testing human chemosensory function throughout the lifespan.
Novel technologies for studying, diagnosing, and treating voice, speech, and language disorders such as laryngeal dystonia (spasmodic dysphonia), phonotrauma, stuttering, dysarthria, developmental language disorders, and aphasia.
Innovative in vivo imaging capabilities that significantly advance visualization, diagnosis, and treatment of communication disorders in the clinic.
Novel systems of augmentative and alternative communication (AAC) for individuals with motor speech impairment, including a brain-computer interface (BCI) prosthesis for communication.
Novel assessments and interventions for late talking children or minimally verbal/ non-speaking individuals.
Novel applications of machine learning / artificial intelligence algorithms in hearing aids, cochlear implants, AAC devices, or for the analysis of voice, speech, and language.
-
Interest Areas:
NIDCR supports small business–led development of technologies and products that translate dental, oral, and craniofacial (DOC) research into clinically actionable solutions across the lifespan. Emphasis is on feasibility, validation, regulatory readiness, and commercialization. Projects should align with NIDCR’s goal to rapidly translate oral health innovations toward clinical impact. Early engagement with program staff is encouraged to ensure alignment with mission and priorities. Scientific areas of interest include:
Targeted DOC diagnostics and therapeutic platforms for tooth-related diseases and periodontal/peri-implant conditions
Orofacial pain assessment and management technologies, including clinical decision support
Oral microbiome-based diagnostics and therapeutic platforms for polymicrobial diseases
AI/ML-enabled predictive health and clinical decision support tools for DOC care
Advanced dental materials, restorative technologies, and digital manufacturing systems
Regenerative medicine technologies for craniofacial and dental tissue reconstruction
Immunomodulatory and precision therapeutic delivery systems for oral and craniofacial conditions
Digital behavioral and monitoring tools targeting DOC outcomes
Real-world evidence and patient outcome data platforms to support clinical adoption, evidence generation, and downstream coverage considerations
Implementation and dissemination technologies for priority-population oral health interventions
Integrated oral–systemic health assessment and intervention platforms
Regulatory and commercialization readiness tooling to support evidence generation, usability, and market adoption
-
Interest Areas:
NIDDK is interested in projects that include robust timelines for commercialization, requisite fundraising, and all required regulatory milestones.
For those projects intended to support completion of research needed for an Investigational New Drug (IND) application, Investigational Device Exemption (IDE), or other regulatory clearance or approval, NIDDK is interested in projects that demonstrate how formal consultation with the U.S. Food and Drug Administration (FDA) has informed the research strategy.
NIDDK is interested in Phase IIB and Commercialization Readiness Pilot projects that propose to continue the process of developing products that ultimately require clinical evaluation and approval by a Federal regulatory agency, and that position the projects for independence from NIH support after the project period.
-
Interest Areas:
NIEHS SBIR/STTR grants help small businesses transform cutting-edge research into developing innovative and commercially viable products such as tools, technologies, assays, or services to translate and communicate environmental health research into improvements in human health. NIEHS SBIR/STTR program uses a combination of research & development, technology transfer, and communication strategies to aid the mission of NIEHS.
The institute’s scientific areas of emphasis include, but are not limited to, the following:
• Tools/technologies such as sensors, computational methods, and exposomics approaches for detecting and assessing human exposures to environmental hazards
• Innovative and/or alternative high-throughput or high-content assays/model systems, computational toxicology approaches, and other related new approach methodologies (NAMs) for toxicity testing and understanding effects on human health and disease
• Tools/methods/applications for evaluating environmental health and safety of engineered nanomaterials and micro/nanoplastics
• Biomonitoring technologies such as point-of-care approaches for personal exposure assessment and exposure mediated biological response biomarkers.
• Intervention technologies and precision environmental health approaches to prevent or reduce human exposures or adverse health effects related to environmental stressors
• Educational materials to promote or support understanding of environmental health science
The NIEHS Superfund Research Program (accepting SBIR applications only) focused on detection and remediation technologies for hazardous substances with relevance to Superfund and/or other contaminated sitesThe NIEHS Worker Training Program (accepting SBIR applications only) also participates
-
Interest Areas:
NIGMS supports the development of technologies to address complex and interdisciplinary research questions in i) basic research, ii) clinical areas that impact multiple organs systems and iii) biomedical workforce development/training through educational activities, that may require additional resources.
-
Interest Areas:
To advance its mission, NIMH supports small businesses to develop technologies, including, but not limited to, the following:
Neurotechnology development to enhance research on brain structure and function
Central nervous system (CNS) drug discovery/development for treating mental disorders – novel drug screening assays, novel compounds and drug targets; Research & Development (R&D) ranging from compound synthesis up to early stage clinical trials
Novel brain modulation methods/devices as potential therapeutics
Biological markers for CNS dysregulation/function and mental illness - objective, measurable biological indicators of physiological or disease processes to further assess replicability, reproducibility, stability, etc. at the subject level
Digital health technologies – as interventions or service delivery tools, to augment clinical care, and/or to enhance clinical research, and clinical trial design/implementation at the subject/patient level
Technologies addressing basic, behavioral, and implementation science related to people living with HIV – including all areas listed above
-
Interest Areas:
NINDS utilizes the SBIR and STTR programs to enable the commercial development of tools and technologies that serve the NINDS mission space. Priority is given to proposals with the greatest potential to advance the NINDS mission.
NINDS is especially interested in the following, in no preferential order:
Novel and innovative technologies that address significant unmet needs
Technologies in development for their first indication or initial market opportunity
Technologies with a compelling need for federal support, such as those at a stage of development requiring de-risking to attract private investment, New Approach Methodologies (NAMs), and those addressing underserved markets including rare and pediatric disease indications
Under-resourced technologies, indications, markets, and geographical regions within the NINDS SBIR/STTR portfolio and mission space
New applicants pursuing their first SBIR/STTR-funded technology
Applicants with a demonstrated track record of advancing technologies through commercialization milestones
For continuation applications, applicants who have achieved intended outcomes under prior funding
Applications demonstrating robust rigor in their approach and preliminary data
-
Interest Areas:
Areas of interest include innovative small business proposals as they relate to NINR research priority areas of intervening on the conditions of daily life that influence health, using multilevel or multi-sectoral approaches to prevent chronic conditions and improve the outcomes of those with chronic conditions, promoting healthy school environments, meaningful engagement of communities at all stages of the research process, and integrating technological advancements, particularly in artificial intelligence (AI), to streamline and improve healthcare outcomes.
-
Interest Areas:
The NLM Small Business Innovation Research (SBIR) and Small Business Technology Transfer (STTR) program supports the development of biomedical informatics tools and methods which are best disseminated through commercialization.
The program aims to encourage small businesses to develop innovative technologies, tools, methods, and software platforms that advance:
Trustworthy, reproducible, and rigorous biomedical AI
Biomedical data infrastructure at scale
Sustainable biomedical reference resources and platform science
Market innovative human-centered use and impact informed biomedical informatics tools and methods
Applications which utilize, integrate, or build upon data, resources, and tools fostered by NLM and NIH supported communities are encouraged.
-
Interest Areas:
ORIP supports research projects to develop technology including, but not limited to, the following:
Create, characterize, or improve models of human disease; and develop new approach methodologies (NAMs) to complement or reduce the use of animal models in research.
Preservation, revival and monitoring of cells, tissue, organs or gametes from model systems.
Validate research models to enhance the rigor and reproducibility of pre-clinical studies.
Devices and technologies required for development and maintenance of conventional and NAM biological model systems, including those for advancing the care, welfare, housing, and management of these models; or sensor and monitoring technologies for the surveillance of models or environmental factors that lead to improved rigor and reproducibility for studies using these models.
Are there any additional benefits I would receive?
Beyond the formal funding award, awardees gain several strategic advantages:
Government Validation and Credibility:
Being selected for an NIH-backed SBIR grant signals technical excellence and alignment with national health and biomedical priorities. This validation builds investor and partner confidence.Enhanced Visibility and Market Recognition:
Awardees are featured in NIH and HHS announcements, helping attract partnerships, media attention, and future contracting opportunities.Access to the Federal Innovation Ecosystem:
Recipients join a national network of researchers and agencies advancing life science innovation, often opening doors to collaborations with NIH laboratories and federal health programs.Stronger Commercial and Exit Potential:
By maturing technology through nondilutive funding, companies strengthen valuation, de-risk commercialization, and increase attractiveness for acquisition or follow-on private investment.
What is the timeline to apply and when would I receive funding?
Applications are accepted each year on January 5th, April 5th, and September 5th. Funding is received approximately 9 months after submission.
Where does this funding come from?
Funding comes from the U.S. Department of Health and Human Services, with statutory set-asides requiring NIH, CDC, and FDA to devote portions of their extramural R&D budgets (3.2% for SBIR, 0.45% for STTR) to support small business innovation.
Who is eligible to apply?
Applicants must be U.S. small business concerns (SBCs) that:
Are organized for profit with a U.S. place of business.
Have ≤ 500 employees including affiliates.
Are > 50% owned by U.S. citizens or permanent residents, qualifying U.S. entities, or combinations thereof.
What companies and projects are likely to win?
Projects that demonstrate:
A clear unmet medical or public-health need,
Strong scientific rationale and feasibility,
High commercialization potential, supported by a realistic market and regulatory strategy, and
Alignment with an NIH Institute’s or CDC/FDA Center’s specific research mission (e.g., infectious disease, digital health, diagnostics, therapeutics, or data analytics).
Competitive applicants often have an early prototype, preliminary data, and a defined path to market adoption.
Are there any restrictions I should know about?
Companies must complete multiple federal registrations (SAM.gov, Grants.gov, eRA Commons, SBA Company Registry) before applying.
Foreign entities are not eligible.
Disclosure of foreign affiliations and compliance with national security screening are mandatory. Currently we do not recommend any sort of foreign affiliation.
How long will it take me to prepare an application?
For a first-time applicant, preparing a competitive submission will likely take 120–200 hours in total.
How can BW&CO help?
Our team specializes in complex federal R&D proposals and can:
Triple your likelihood of success through proven strategy and insider-aligned proposal development
Reduce your time spent on the proposal by 50–80%, letting your team focus on technology and operations
Ensure you are targeting the best opportunity for your project and positioning your company for long-term growth.
Additional Resources
Webinar - NIH Grant Admin for Academic Spin-Outs & First-Time Applicants
DOI & IARPA - EMERGING TECHNOLOGY ACCELERATOR (ETA) PROGRAM ANNOUNCEMENTDOI-ETA-FY26-30
Deadline: Rolling Deadline
Funding Award Size: $500k - $5m
Description: Apply for IARPA’s ETA Program (DOI-ETA-FY26-30). Rolling white paper submissions for AI, geospatial, and advanced R&D projects.
Below is a brief summary. Please check the full solicitation before applying (link in resources section).
Executive Summary:
The Emerging Technology Accelerator (ETA) Program Announcement (DOI-ETA-FY26-30) is a multi-program IARPA funding vehicle supporting high-risk, high-payoff R&D across multiple active programs (e.g., ARCADE, COSMIC, DECIPHER, LocUS). Awards are made as Prototype Other Transaction Agreements (OTs) through a competitive, white paper–first process.
There is no fixed submission deadline — White Papers per Program: Continuous, after the posting of Q&As (Preferred).
This is a rolling opportunity, but programs can close once sufficient white papers are received. That creates real urgency: if you are aligned, you should apply as soon as possible before a program is re-labeled “Not Active.”
How much funding would I receive?
Not specified in the solicitation.
The Government will make multiple Prototype OT awards
Funding depends on:
Quality of proposals
Availability of funds
Awards may be:
Partial (only parts of proposals funded)
Incremental or phased
No award size ranges or total program value are provided.
Research Topics:
-
ARCADE transforms and accelerates electrical circuit design within the Intelligence Community (IC) by leveraging Artificial Intelligence (AI) to develop an intelligent, comprehensive AI-knowledge assistant that extracts key information from vast technical documentation and enables engineers to perform quick, intuitive queries to meet the speed of mission.
The technical information ingested by ARCADE will include text, datasheets, diagrams, schematics, tables, and graphs. ARCADE extracts crucial details about electrical components, their specifications and interfaces to compile them into a comprehensive searchable knowledge platform.
Going beyond a simple search engine, ARCADE aims to suggest and recommend optimal components based on design requirements, constraints, and performance parameters as specified through user-defined prompts. This capability enables engineers to perform swift, targeted queries, dramatically reducing the time it takes to find, compare, and select suitable parts. It also aims to help identify optimal components and potential alternatives more efficiently by providing comparison tables and explanations for why specific components were selected, effectively saving engineers from manually sifting through thousands of documents. Ultimately, ARCADE will lead to faster, more accurate, and more robust circuit designs, ensuring Government missions can be deployed with unprecedented speed and reliability.
-
The aim of the Commercial Observation for Spatio-temporal Monitoring for Indications of Change (COSMIC) program is to formulate a methodology to leverage commercial remote sensing technologies and open source geolocated information to generate pseudo-persistent data (PPD). This will be done by combining and translating complex and novel data, such as nonnadir imagery and non-Red,Green, Blue (RGB) spectral bands, using Artificial Intelligence (AI) and computer vision-based methodologies into a layered, temporal geospatial model understandable by commercial agentic AI systems. COSMIC will enable the development of an agentic AI analytic system trained by commercial vendors and equipped to answer intelligence questions by bridging the gap between the Intelligence Community (IC) data characteristics and the simpler solutions offered by commercial vendors.
COSMIC will foster routine updating and modelling of baseline geospatial information in areas through multi-source, persistent surveillance. New sensors will fluidly be incorporated into the generation of layered geospatial models as constellations and sources change over time. In addition to improving the temporal resolution of layered geospatial models, COSMIC also aims to reduce resource demands by streamlining the derivation of actionable intelligence from these models. By integrating commercial remote sensing data with existing geospatial information, the program aims to create a harmonized and up-to-date representation of the physical world that can be used by agentic processes to answer questions relevant to the IC.
-
Analysts often struggle to understand specialized language (e.g., slang, jargon, technical terminology) in various situations where dictionary definitions are not readily available, such as:
• Non-English research articles with novel technical concepts and terms
• Communications using slang
• Undefined acronyms used within limited contexts
• Web forum posts using coded language to mask illicit activities
In these and similar contexts, analysts dedicate significant effort to triaging content pertinent to their domain of interest and understanding the meaning of unknown or novel specialized terms used within that domain. Adding to this challenge, language can change quickly, and adversaries can rapidly adapt their language to evade detection.
The Decipher program’s goal is to create capabilities to detect and define specialized language in diverse, multilingual text collections. In Decipher, “specialized language” refers to single or multiword expressions that are difficult to disambiguate (e.g., acronyms, terminology with multiple meanings), are used to deliberately obfuscate interpretation (e.g., coded language), or for which accurate translations or explanations are not readily available (e.g., emergent jargon or slang) to typical non-expert users. Decipher will flag and extract candidate specialized terms in a document or corpus and then will provide candidate plain language translation and annotation of specialized terms, including jargon, slang, and acronyms. The program will also develop technology to annotate text with relevant social and contextual factors, capturing nuanced meaning, as well as to detect concept drift by monitoring use of terminology as it evolves over time.
-
The LocUS program aims to create technology that automatically and accurately geolocates multimedia content by maximally leveraging audio and visual information. LocUS will improve the geolocation capabilities of the Intelligence Community (IC) considerably beyond imageryonly methods and thereby increase the volume of content that can be accurately geolocated. This program will increase analysts’ ability to rapidly and accurately determine where a video, image, or audio clip was collected in the absence of accurate metadata indicating location. Applications for national security include human trafficking interdiction, hostage recovery, localization of malign actors using social media or confiscated devices, and other intelligence and law enforcement use cases.
-
The intelligence community (IC) would benefit from the ability to diagnose, from open-source data, medical conditions in individuals and populations. This ability would enable, e.g., monitoring of the spread of health threats (disease, chemical accidents or attacks, environmental toxins, etc.) and other medical intelligence analyses. The MOVES program aims to demonstrate the feasibility of this long-term goal by addressing a subset of the challenges associated with generalized diagnosis from video.
The MOVES program will focus on diagnoses of neurological conditions that typically affect people’s movement and demonstrate that it is feasible to diagnose such conditions from challenging input video that may:
• Be taken from non-ideal angles
• Include subjects wearing a wide variety of clothing styles
• Show partially obstructed subjects
The program requirements are selected to ensure a path to rapid adoption and trust in the algorithms’ performance by medical professionals. Key challenges include the nature of the videos as described above, especially finding movements that are diagnostic of conditions, differentiating between similar symptoms of different disorders, and providing enough information to the medical professionals about how the diagnosis was made so that they can verify the diagnosis and build confidence in the algorithm performance.
Are there any additional benefits I would receive?
Yes:
Potential follow-on production Contract or OT if prototype is successful
Direct engagement with IARPA and Intelligence Community stakeholders
Access to Government-furnished data (program-dependent)
Independent Test & Evaluation (T&E) feedback throughout development
What is the timeline to apply and when would I receive funding?
Application timeline:
White Papers per Program: Continuous, after the posting of Q&As (Preferred)
Full proposals: By invitation only
Process:
Submit White Paper
Government evaluates for viability
If selected → invited to submit full proposal
If selected → negotiation → award
Award timing:
Not specified in the solicitation.
Where does this funding come from?
Department of the Interior (DOI), Interior Business Center (IBC)
In partnership with IARPA (Intelligence Advanced Research Projects Activity)
Authority:
Issued under 50 U.S.C. § 3024(m)(6) for Prototype OT agreements
Who is eligible to apply?
Eligible:
All responsible sources capable of meeting requirements
U.S.-based entities (prime must be U.S.)
Teams including:
Small businesses
Non-traditional defense contractors (NDCs)
Non-profits
Foreign participation:
Allowed only as part of a U.S.-based team
Not eligible:
Government agencies
FFRDCs
UARCs
Government-affiliated organizations with privileged access
What companies and projects are likely to win?
Based on evaluation criteria, winning proposals will:
Demonstrate innovative, high-risk/high-payoff technical approaches
Clearly align with specific program objectives
Show feasible execution plans with defined milestones
Include strong technical teams and capabilities
Address technical risks with mitigation strategies
Offer IP terms that allow Government transition
The Government prioritizes:
Scientific merit
Relevance to IARPA mission
Resource realism
Are there any restrictions I should know about?
Yes — several important ones:
Submission restrictions
One program per white paper
Must follow strict formatting and page limits
Funding restrictions
No facility construction
No commercialization costs
Technical restrictions
Classified proposals are not accepted
IP & data
Government requires sufficient rights for transition
Must disclose IP ownership and restrictions
Compliance requirements
NSPM-33 research security disclosures required
Potential foreign influence review and mitigation
How long will it take me to prepare an application?
Requirements include:
White Paper (up to ~8 pages technical content)
If invited:
Full technical proposal (≤15 pages)
Detailed cost proposal
Multiple compliance attachments
This is a moderate-to-high effort application, especially at full proposal stage.
How can BW&CO help?
BW&CO can support:
Program selection (which ETA program to target)
White paper strategy and positioning
Technical narrative development aligned to IARPA evaluation criteria
Full proposal development (if invited)
IP, compliance, and structure alignment
End-to-end submission management
Additional Resources
ARPA-H - SBIR/STTR Broad Agency Announcement (BAA)
Deadline: July 10, 2026
Funding Award Size: $600k - $3.5m
Description: Apply for ARPA-H SBIR funding up to $3.5M. Open to health and biotech startups. Deadline: July 10, 2026 (11:59PM ET).
Below is a brief summary. Please check the full solicitation before applying (link in resources section).
Executive Summary:
This is the ARPA-H SBIR/STTR Broad Agency Announcement (BAA) for high-impact healthcare technologies across seven topic areas. It uses a two step application process (Solution Summary → Technical Presentation) and supports Phase I, Direct-to-Phase II, and Fast Track awards.
There is strong urgency to prepare early, but note:
The Solution Summary Due: July 10, 2026 (11:59PM ET)
The solicitation is currently a draft and not yet accepting applications
Because ARPA-H uses a gated, competitive process with strict technical novelty requirements, companies should begin positioning immediately—especially given topic-specific windows and evolving amendments.
How much funding would I receive?
Funding depends on phase and topic. Typical amounts are:
Phase I: up to $600,000
Phase II: up to $3,500,000
Some topics specify:
~$600k (Phase I) and $3.5M (Phase II) (Topics 1–4, 7)
$3.5M (Phase II only) (Topics 5–6)
All awards are issued as Firm-Fixed-Price (FFP) contracts with milestone-based payments
Research Topics:
-
The purpose of this topic is to discover new biomarkers that provide women with actionable data for fertility planning. Results from this work will help inform the program manager regarding the feasibility of future programs focused on enhancing natural fertility before the need of IVF and guiding the development of women’s health monitoring and improvement tools. This work will develop a diagnostic test that can assess fertility status and generate an estimated timeline for the onset of infertility. This topic seeks to develop a test that is affordable, suitable for at least annual use, and provides user-friendly results for patients and care teams to support childbearing decisions.
-
The purpose of this topic is to develop surgical glues with antimicrobial properties to combat infections due to surgery. In addition, the novel multifunctional surgical glue will also have desired properties such as controllable reversibility and degradability and be tissue/organ agnostic to stop bleeding with unknown sources. Overall, successful completion of this SBIR project will not only support the clinical implementation of bioprinted organs but also provide novel solutions to tackle unmet clinical needs in managing surgical leaks and infections and reduce overall medical costs.
-
The purpose of this topic area is to catalyze the development of a universal, “plug-and-play” synthetic biology platform that enables next-generation microbial chassis capable of performing a broad array of programmable functions. While this solicitation primarily uses toxin removal as a proof-of-concept in relation to chronic disease management, the platform is intended to be adaptable to a range of challenges across industries such as environmental remediation, biomanufacturing, agriculture, holistic medicine, and therapeutic discovery. The broader goal is to create a stable, reliable, and easily reprogrammable microbial platform that demonstrates potential for cross-sector impact beyond the initial use case.
-
The purpose of this topic aims to advance progress in the endometriosis field by identifying and commercializing non-invasive therapeutics that address the root cause of the disease. Proposers are expected to develop a first-of-its-kind, non-invasive therapy capable of reducing the size of endometriosis lesions, deactivating endometriosis tissue, and/or preventing regrowth thereby ideally achieving curative outcomes. Additionally, proposers need to showcase a solution that has precise, targeted specificity, ensuring the treatment accurately locates and addresses endometriosis lesions without causing adverse effects elsewhere in the body.
-
The purpose of this topic supports the advancement, commercialization, and translation of technologies that originated from ARPA-H funded efforts. It is intended to help small businesses and startups develop viable products based on these technologies. ARPA-H’s goal is to give small businesses an off-ramp to finish developing their technology/product, explore secondary or interim applications of the technology, and time to achieve self-sufficiency.
-
The overall purpose of this topic is to spur the development of novel, rapid diagnostic assays for multi-system autoimmune disease, which represents an unmet healthcare need. Moreover, in its ideal embodiment this diagnostic test might allow typical primary care physicians to diagnose and predict tissue-specific autoimmune disease manifestations, thereby streamlining referral of the patient to a specialist. This goal is made more feasible by recent technological developments incility to detect tissue-specific signatures of immune-mediated stress by assessing circulating cells and/or tissue-specific molecular products.
-
The overall purpose of this topic aims to take a first step toward AI-assisted intracranial microsurgery, which will ameliorate patient outcomes as described in point 5 above, by creating a high-resolution, physically and anatomically accurate virtual human brain.
Are there any additional benefits I would receive?
Yes. ARPA-H provides hands-on commercialization support, including:
Entrepreneur-in-Residence (EIR) program (strategic guidance on IP, regulatory, market strategy)
Regulatory and reimbursement support
Customer discovery and stakeholder introductions
I-Corps program participation (optional)
Potential Technical and Business Assistance (TABA) funding
Support is not guaranteed and is provided at ARPA-H’s discretion
What is the timeline to apply and when would I receive funding?
Key Dates
Solution Summary Due: July 10, 2026 (11:59PM ET)
Technical Presentation (if invited): September 9, 2026 (11:59PM ET)
Process Timeline
Stage 1: Submit Solution Summary (4–6 pages)
Stage 2: If invited → Technical Presentation + full materials
ARPA-H response:
~90 days after topic close for Stage 1 decision
~30 days after presentation for final decision
Awards targeted within ~180 days of topic closing
Funding Timing
Payments are quarterly milestone-based, not upfront
Where does this funding come from?
Funding comes from:
Advanced Research Projects Agency for Health (ARPA-H)
Under the SBIR/STTR program, authorized by the U.S. Small Business Act
Within the U.S. Department of Health and Human Services (HHS)
The program is designed to fund transformational health technologies with commercialization potential
Who is eligible to apply?
Core Eligibility
You must be a Small Business Concern (SBC) that:
Has ≤500 employees
Is majority U.S.-owned
Performs work in the United States
SBIR Requirements
PI >50% employed by small business
Work share:
Phase I: ≥66% by small business
Phase II: ≥50% by small business
STTR Requirements
Must include a research institution partner
Work share:
≥40% small business
≥30% research institution
Additional Requirements
SAM.gov registration
SBA Company Registry
Foreign affiliation disclosures
Required certifications at submission
What companies and projects are likely to win?
ARPA-H is explicitly looking for:
Non-incremental, breakthrough technologies
Solutions with clear technical novelty and feasibility
Teams with:
Proven ability to execute
Commercialization capability
Projects that:
Address major unmet health needs
Have a credible path to market and impact
Can reach a commercial inflection point
Strong proposals demonstrate:
Clear technical milestones and risk mitigation
Evidence-backed claims
A viable commercialization plan
Incremental or purely academic work is unlikely to be competitive
Are there any restrictions I should know about?
Key restrictions include:
No incremental R&D—must be transformative
No Phase III proposals
Must follow topic-specific eligibility (phase/type)
Strict foreign affiliation disclosure and national security review
Funding may be denied for:
Security risks
Undisclosed foreign relationships
Proposal cap: max 6 submissions per fiscal year across HHS
Other constraints:
Must submit through ARPA-H Solutions site only
No email or paper submissions accepted
How long will it take me to prepare an application?
Typical effort:
Stage 1 (Solution Summary):
4–6 pages
~1–3 weeks for a prepared team
Stage 2 (if invited):
Full technical package + presentation
~3–6+ weeks
Additional prep time may be required for:
Registrations (SAM can take >14 business days)
Certifications and compliance documentation
How can BW&CO help?
BW&CO can support across the full lifecycle:
Topic selection and win strategy positioning
Translating your technology into ARPA-H-aligned narratives
Writing:
Solution Summary
Technical presentation materials
Building commercialization strategy aligned to ARPA-H expectations
Preparing for technical Q&A and evaluation criteria
Managing compliance and submission requirements
Additional Resources
Arcane Thunder 27 (AT 27)
Deadline: May 22nd, 2026
Funding Award Size: N/A
Description: Submit your technology to the U.S. Army’s Arcane Thunder 27 (AT27) RFI. Participate in multi-domain experiments across AI, cyber, EW, autonomy, and communications. Deadline: 22 May 2026.
Below is a brief summary. Please check the full solicitation before applying (link in resources section).
Executive Summary:
This is an RFI (Request for Information), not a funding opportunity, but it is a critical gateway to Army experimentation and potential follow-on contracting. The U.S. Army is seeking cutting-edge technologies for Arcane Thunder 27 (AT27), a major multi-domain experimentation campaign.
If selected, your technology may be invited to participate in field demonstrations and exercises with operational units. This is a high-visibility pathway to engage directly with the Warfighter and DoD stakeholders.
Submission deadline: 22 May 2026 : 22:59 CDT.
Missing this deadline means waiting for future cycles—there is no guarantee of a re-open.
How much funding would I receive?
This RFI does not include funding, but funding would shortly follow.
What could I use the funding for?
AI-Enabled Command & Control
Edge-deployed AI for decision support, wargaming, and risk analysis
Automated synchronization across units and systems
AI models that operate in degraded or denied environments
Cyber, Electronic Warfare & Information Operations
RF, cyber, and information effects (detect, disrupt, deceive)
AI-driven emitter identification and behavior modeling
Integrated cyber/EW payloads across platforms
Multi-Domain Sensing & Targeting
Sensor fusion across RF, EO/IR, SAR, and other modalities
Real-time targeting and geolocation (TDOA/FDOA/DF)
Adaptive sensor tasking and AI-enabled targeting
Resilient Communications & Networking
Low probability of intercept/detection (LPI/LPD) communications
Self-healing mesh networks across air, ground, and space
Cross-domain data transfer (unclassified to higher classification)
Autonomy, Robotics & Swarming
Multi-platform control with single operator
Adaptive swarm behavior based on mission and threat
Autonomous detection, tracking, and targeting
Additive Manufacturing & Edge Modularity
Field-ready 3D printing for parts and payloads
Modular, plug-and-play payload architectures
In-theater reconfiguration and resupply
Operational Simulation & Decision Tools
Live, Virtual, Constructive (LVC) environments
Digital twins and mission rehearsal tools
End-to-end visualization of sensor-to-shooter workflows
Supporting Capability Areas
Counter-UAS systems
Space-based communications and sensing
Defensive cyber operations
Signature reduction (RF, visual, EMS)
Threat replication and red-teaming tools
Are there any additional benefits I would receive?
Yes—this opportunity is about access and validation, not capital:
Invitation to Army-led field experiments and demonstrations
Direct engagement with:
Warfighters
DoD R&D organizations
Combatant Commands and other agencies
Real-world testing in contested, denied, and austere environments
Opportunity for follow-on contracting actions
Visibility into how your product performs in multi-domain operations
What is the timeline to apply and when would I receive funding?
Submission deadline: 22 May 2026 : 22:59 CDT.
Key milestones:
NLT 30 September 2026: Down-select notifications
Late 2026: Planning conferences and interviews
Early 2027: Final planning and risk reduction
Apr – Jun 2027: Field exercises (CONUS and OCONUS)
Funding timeline: Not specified in the solicitation.
Where does this funding come from?
Not applicable.
Issued by the U.S. Army DEVCOM C5ISR Center for experimentation purposes.
Who is eligible to apply?
Industry
Academia
Individuals
Laboratories
Must:
Submit via Vulcan-SOF
Provide a Scout Card + Technology Quad Chart
Keep all submissions unclassified
What companies and projects are likely to win?
Selections favor technologies that are:
Relevant to current military missions
Technically mature and deployable
Adaptable across multiple use cases
Aligned to multi-domain operations
Are there any restrictions I should know about?
Do NOT submit proposals — only Scout Cards
No classified information allowed
Must disclose ITAR/EAR/OFAC restrictions
Data generated becomes U.S. Government property
Must use required formats or risk rejection
How long will it take me to prepare an application?
Expect to prepare:
Scout Card (per technology)
Quad Chart
Technical specs (SWaP, power, spectrum, etc.)
How can BW&CO help?
BW&CO can support across all phases of this CSO:
Refine your positioning against Army priority areas
Translate your tech into a high-impact Scout Card
Ensure compliance with submission and formatting rules
Increase likelihood of selection for demonstration
Additional Resources
United States Transportation Command (USTRANSCOM) - Commercial Solutions Opening (CSO) - HTC71126SCSO1
Deadline: Rolling Deadline
Funding Award Size: $500k - $5m
Description: Apply to the USTRANSCOM CSO (HTC71126SCSO1), a continuously open funding opportunity for IT, cybersecurity, and logistics solutions. Open until February 1, 2036.
Below is a brief summary. Please check the full solicitation before applying (link in resources section).
Executive Summary:
The United States Transportation Command (USTRANSCOM) Commercial Solutions Opening (CSO) (Solicitation Number: HTC71126SCSO1) is a continuously open funding pathway for companies developing commercial technologies that support global mobility, logistics, IT, and cybersecurity missions. Unlike traditional grants, this is a flexible acquisition vehicle that can lead directly to contracts or Other Transaction (OT) agreements.
This opportunity is continuously open until 1 February 2036 , with new Areas of Interest (AoIs) released on a rolling basis—some with dedicated funding and defined submission windows. If your solution aligns with USTRANSCOM’s mission, you can submit at any time, but Specific AoIs may have limited windows and should be monitored closely on SAM.gov.
How much funding would I receive?
Funding typically ranges from $500k to $5m.
What could I use the funding for?
1. AoI-901: Information Technology (IT) and Cybersecurity Solutions:
USTRANSCOM seeks IT and cybersecurity solutions that provide unique capabilities or more efficient approaches not currently in use by USTRANSCOM. These solutions should modernize enterprise systems, enhance operational efficiency, and strengthen security posture while meeting stringent security standards to support global integrated mobility operations.
Representative examples include:
• Cloud-based IT services and architecture
• Cybersecurity defense and threat detection systems
• Transportation management systems
• Artificial intelligence and machine learning applications
1.1. Security and Compliance Requirements:
All IT solutions must address: compliance with Defense Federal Acquisition Regulation Supplement (DFARS) 252.204-7012 for unclassified systems, adherence to National Industrial Security Program Operating Manual (32 CFR Part 117) for classified systems, implementation of Risk Management Framework processes, support for Authority to Operate requirements, and incident reporting capabilities per USTRANSCOM requirements.
1.2. Technical Data and Software Rights:
Offerors must identify any intellectual property, data rights restrictions, and licensing requirements associated with their proposed solutions. Submissions should clearly outline how technical data and software rights will be managed to ensure compatibility with USTRANSCOM systems and compliance with applicable regulations.
2. AoI-902: Transportation and Logistics Optimization:
USTRANSCOM seeks solutions that optimize transportation and logistics operations, improve supply chain resilience, and enhance global distribution capabilities. Submissions should offer unique approaches or efficiencies not currently utilized by USTRANSCOM to address operational challenges, visibility, and scalability in support of the global mobility mission.
Representative examples include:
• Supply chain resilience and risk management
• Real-time tracking and visibility platforms
• Predictive analytics for logistics decision support
• Automated transportation and cargo handling systems
Are there any additional benefits I would receive?
Access to FAR-based contracts or OT Agreements for Prototype Projects
Ability to work directly with USTRANSCOM on mission-critical challenges
Streamlined acquisition under DFARS Subpart 212.70
Potential for multiple awards or follow-on opportunities
No additional non-monetary benefits are explicitly specified beyond contracting pathways.
What is the timeline to apply and when would I receive funding?
CSO open period: continuously open until 1 February 2036
General AoIs:
Submissions accepted at any time
No guaranteed response timeline
Specific AoIs:
Posted on SAM.gov with defined submission windows
Timelines vary by AoI
Process timeline (not fixed):
Phase 1 – Solution Brief submission
Phase 2 – Presentation/Pitch (if invited)
Phase 3 – Full Proposal (if invited)
Award decision
Timing for award decisions and funding is not specified in the solicitation.
Where does this funding come from?
Funding comes from the United States Transportation Command (USTRANSCOM), part of the Department of War (DoW) .
Awards are executed under:
Federal Acquisition Regulation (FAR) Part 12 contracts
10 U.S.C. 4022 Other Transaction (OT) authority
Who is eligible to apply?
Eligibility requirements explicitly include:
Must provide commercial products, technologies, or services
Must be a registered entity in SAM.gov to receive an award
What companies and projects are likely to win?
USTRANSCOM evaluates submissions based on:
Alignment to mission needs
Technical feasibility
Innovation and uniqueness
Milestone schedule realism
Prior experience delivering similar solutions
Affordability and return on investment
Projects most likely to advance:
Demonstrate working capability (not conceptual only)
Provide clear value over existing systems
Show credible delivery plans and pricing
Align directly with AoIs such as IT/cybersecurity or logistics optimization
Are there any restrictions I should know about?
Key restrictions include:
Strict submission format requirements (e.g., Scout Card + video for General AoIs)
Video must be ≤ 5 minutes and demonstrate working capability
Non-compliant submissions will not be evaluated
Submission costs are not reimbursed unless explicitly stated
Must comply with:
DFARS cybersecurity requirements
National Industrial Security Program (for classified systems)
Risk Management Framework and Authority to Operate processes
How long will it take me to prepare an application?
Not explicitly specified, but based on requirements:
Phase 1 includes:
Scout Card submission
5-minute demo video OR up to 6-page white paper (for Specific AoIs)
Preparation time will vary depending on:
Readiness of a working prototype
Ability to produce a demonstration video
Pricing and delivery estimates
How can BW&CO help?
BW&CO can support across all phases of this CSO:
Identify the right AoIs and timing strategy
Develop high-impact Solution Briefs and demo narratives
Structure submissions to align with evaluation criteria
Prepare Phase 2 pitches and Phase 3 proposals
Ensure compliance with format, pricing, and technical requirements
Additional Resources
xTech|Phantum Competition (ARM26BX01-NP003)
Deadline: May 6, 2026
Funding Award Size: $300k
Description: U.S. Army xTech Phantum Competition offers small businesses a path to $300K SBIR funding for quantum sensors and photonics. White papers due May 6, 2026.
Below is a brief summary. Please check the full solicitation before applying (link in resources section).
Executive Summary:
The U.S. Army is seeking small businesses developing quantum sensors and photonics technologies through the xTech|Phantum Competition. This is a gated pathway to SBIR funding—only competition winners can submit a Phase I proposal. Companies can earn prize money, engage directly with the Department of War, and position themselves for follow-on SBIR funding.
White paper submission deadline: May 6, 2026
How much funding would I receive?
Phase I SBIR:
Up to $300,000
6-month period of performance
Prize money:
Not specified in the solicitation
What could I use the funding for?
Phase I funding is for feasibility and concept development, including:
Demonstrating technical advantage over existing solutions
Developing concept plans aligned with Army modernization priorities
Providing supporting technical literature and performance data
Building a commercialization strategy (defense and commercial markets)
Creating a technology development roadmap
Delivering a concept demonstration at the end of Phase I
Technology focus areas include:
Quantum sensors and quantum clocks for non-GPS PNT
Quantum RF sensors
Quantum electromagnetic sensors
Photonics for communications and edge processing
Are there any additional benefits I would receive?
Direct engagement with the Department of War (DoW)
Feedback from Army stakeholders to accelerate technology development
Entry into the Army’s Science & Technology ecosystem
Eligibility to submit a Phase I SBIR proposal (only if selected as a winner)
What is the timeline to apply and when would I receive funding?
White paper submission deadline: May 6, 2026
xTech|Phantum competition selection timeline: Not specified
Phase I SBIR award timing: Not specified
Phase I performance period: 6 months
Where does this funding come from?
Assistant Secretary of the Army for Acquisition, Logistics and Technology (ASA(ALT))
U.S. Army Directorate for Strategy & Transformation (DAMI-ST)
Delivered via the xTech|Phantum Competition and Army SBIR program
Who is eligible to apply?
Must participate in the xTech|Phantum competition
Only competition winners are eligible to submit a Phase I SBIR proposal
Additional eligibility requirements are not specified in the provided document.
What companies and projects are likely to win?
The Army is prioritizing companies developing:
Quantum technologies enabling non-GPS positioning, navigation, and timing
Quantum RF sensors with improved sensitivity, bandwidth, and SWaP
Electromagnetic sensors detecting low-power or non-RF signals
Photonics systems for secure, high-speed communications and edge computing
Strong applications will:
Demonstrate clear technical feasibility and differentiation
Show dual-use commercial potential
Align directly with Army modernization priorities
Provide credible pathways to prototype and field deployment
Are there any restrictions I should know about?
Only xTech|Phantum competition winners can submit a Phase I SBIR proposal
Proposals from non-participants or non-winners will not be evaluated
CMMC requirement: Level 1
Other restrictions (e.g., cost share, ownership constraints) are not specified.
How long will it take me to prepare an application?
Not specified in the solicitation
Application requires submission of a white paper by May 6, 2026
How can BW&CO help?
BW&CO can support across both stages of this opportunity:
xTech white paper strategy and drafting
Positioning your technology against Army priorities
Translating commercial tech into defense use cases
Preparing a competitive Phase I SBIR proposal (if selected)
Building commercialization and transition plans aligned with Army expectations
Additional Resources
Development of Candidate Medical Countermeasures (MCMs) and Technologies Against Chemical or Radiation/Nuclear (CRN) Threats
Deadline: October 9th, 2026
Funding Award Size: est. $500k - $2m
Description: NIH/NIAID funding for medical countermeasures against chemical and radiation threats. Supports preclinical R&D, diagnostics, and post-exposure treatments. Deadline: October 9, 2026.
Below is a brief summary. Please check the full solicitation before applying (link in resources section).
Executive Summary:
This NIH opportunity (RFA-AI-27-014) supports the development of medical countermeasures (MCMs) and enabling technologies to address chemical and radiation/nuclear (CRN) threats in civilian settings. The program is administered by NIAID through the Radiation and Nuclear Countermeasures Program (RNCP) and Chemical Countermeasures Research Program (CCRP). It is designed to fund early and preclinical work that can diagnose, mitigate, or treat injuries following exposure.
This is a forecasted opportunity with an Estimated Application Due Date: October 9, 2026. Founders working in radiological, nuclear, or chemical threat preparedness should begin positioning now, as this is a complex NIH cooperative agreement with long lead times.
How much funding would I receive?
Funding amounts are not specified in the solicitation, but we anticipate funding to range from $500k - $2m.
What could I use the funding for?
Funding supports research and development of medical countermeasures and enabling technologies addressing CRN threats, including:
Radiation and Nuclear Countermeasures Program (RNCP):
Radiation-focused models
Biomarkers of radiation damage
Devices to assess and predict injury
Products to improve survival and reduce morbidity across organ systems
Chemical Countermeasures Research Program (CCRP):
Preclinical development of products
Technologies to mitigate or treat injury after exposure to Chemicals of Concern
Solutions designed for post-exposure, civilian mass casualty settings
All work must align with developing capabilities to diagnose, mitigate, or treat acute and delayed effects of radiation or chemical exposure during or after public health emergencies.
Are there any additional benefits I would receive?
Not specified in the solicitation.
What is the timeline to apply and when would I receive funding?
Estimated Post Date: July 10, 2026
Estimated Application Due Date: October 9, 2026
Estimated Award Date: July 1, 2027
Estimated Project Start Date: July 1, 2027
Additional timeline details are not specified in the solicitation.
Where does this funding come from?
This funding is provided by the National Institute of Allergy and Infectious Diseases (NIAID) on behalf of the NIH.
It is authorized under:
Sections 301 and 405 of the Public Health Service Act (42 USC 241 and 284)
Federal Regulations: 42 CFR Part 52 and 2 CFR Part 200
The program is supported by a congressional mandate (Public Law 109-149, Dec. 30, 2005) to advance research addressing chemical and radiological threats.
Who is eligible to apply?
For-profit:
Small businesses
For-profit organizations other than small businesses
What companies and projects are likely to win?
Projects that align closely with the stated program goals, including:
Development of medical countermeasures for radiation or chemical exposure
Technologies addressing post-exposure treatment in civilian mass casualty scenarios
Preclinical-stage innovations with clear pathways to mitigating injury or improving survival
Tools for diagnostics, biomarkers, or injury assessment
Further selection criteria are not specified in the solicitation.
Are there any restrictions I should know about?
Funding instrument is a cooperative agreement
No cost sharing or matching requirement
Additional restrictions are not specified in the solicitation.
How long will it take me to prepare an application?
Given this is an NIH cooperative agreement focused on preclinical and translational research, preparation timelines are typically substantial, but exact expectations are not specified in the solicitation.
How can BW&CO help?
BW&CO can support:
Translating your technology into NIH-aligned positioning
Mapping your solution to RNCP or CCRP priorities
Structuring a competitive preclinical development narrative
Managing the full application process ahead of the October 9, 2026 deadline
Additional Resources
AFRL - Multi-Spectrum Defensive Electronic Warfare (MSDEW) Advanced Research Announcement (ARA)
Deadline: Rolling Submission Deadline
Funding Award Size: $20M–$100M
Description: AFRL MSDEW ARA offers $20M–$100M awards for electronic warfare, sensor fusion, and defense systems. Rolling calls open through 13 JULY 2027.
Below is a brief summary. Please check the full solicitation before applying (link in resources section).
Executive Summary:
This is a rolling Air Force Research Laboratory (AFRL) Advanced Research Announcement (ARA) for the Multi-Spectrum Defensive Electronic Warfare (MSDEW) program. It does not accept proposals directly—you must apply through future “calls” released under this ARA.
The ARA remains open for calls until 13 JULY 2027. Each call will define its own requirements, funding, and deadlines. If you are building advanced electronic warfare, sensor fusion, or multi-domain defense technologies, this is a long-running, high-budget entry point into AFRL funding—but you must actively monitor and respond to individual calls as they are released.
How much funding would I receive?
Total program value: $396,600,000.00
Typical award size:
$20,000,000.00 to $100,000,000.00 per award
Number of awards:
Multiple awards expected
No limit per offeror
The Air Force reserves the right to exceed these amounts if in its best interest
What could I use the funding for?
Funding supports R&D and prototyping in multi-spectrum electronic warfare systems, including:
Sensor development across RF and electro-optical domains
Threat warning and countermeasure systems
Integration of multi-sensor systems across air, space, and cyber
Modeling, simulation, and analysis (MS&A)
Testing, experimentation, and demonstration (including flight tests)
Software development (signal processing, algorithms, interfaces)
System architecture (open systems, integration frameworks)
Transitioning technologies to operational systems
Core technical areas include:
Electro-optic & multi-spectrum countermeasures
Directed energy threat warning
Missile warning systems
Cyber-secure and open EW systems
Are there any additional benefits I would receive?
Potential access to large-scale DoD test environments, including flight testing
Opportunity to transition technologies into Air Force operational systems
Flexible award structures:
FAR-based contracts
Other Transactions (OTs)
Ongoing opportunity to compete for multiple awards over several years
What is the timeline to apply and when would I receive funding?
ARA open through: 13 JULY 2027
Proposal deadlines:
To be determined (TBD) on individual calls
Award timing:
TBD per individual call
Notification typically ~30 days after proposal submission
Period of performance:
TBD per individual call
Where does this funding come from?
Air Force Research Laboratory (AFRL), Sensors Directorate (AFRL/RYW)
Funding supports U.S. national defense and electronic warfare capability development
Who is eligible to apply?
Unrestricted solicitation
Eligible applicants:
Businesses of all sizes
Educational institutions
No cost sharing required
Additional notes:
FFRDCs subject to eligibility determinations
Foreign participation:
Not anticipated but may be allowed case-by-case
No limit on number of proposals per offeror
What companies and projects are likely to win?
Proposals are evaluated primarily on:
Technical Merit (highest priority):
Clear understanding of the problem
Strong, feasible technical approach
Relevant experience and qualified team
Ability to advance the state of the art
Potential to transition to operational use
Cost/Price (secondary):
Realistic and justified cost structure
Projects that are most competitive will:
Integrate multiple sensing modalities
Demonstrate real-world applicability (lab + field/flight testing)
Align with Air Force mission needs
Enable transition to future defense systems
Are there any restrictions I should know about?
Many awards will require Top Secret security capabilities
Export control (ITAR/EAR) may apply
Data rights heavily favor the Government (including unlimited rights for government-funded work)
Strict proposal formatting and submission requirements
Accounting system requirements for cost-reimbursement contracts
Compliance with:
OPSEC
Program Protection Plan (PPP)
Safety regulations
Foreign involvement may be restricted per call
How long will it take me to prepare an application?
Not specified in the solicitation
However:
Proposals are submitted in response to individual calls
Each call will define:
Page limits
Technical and cost requirements
Submissions include both technical/management and cost/business volumes
How can BW&CO help?
BW&CO can support you across the full lifecycle of this ARA:
Monitor and identify relevant MSDEW calls
Position your technology against AFRL priorities
Develop compliant technical and cost proposals
Structure OT vs FAR contract strategy
Build transition narratives aligned to Air Force needs
Manage complex submission requirements and timelines
How much would BW&CO Charge?
Our services range from an hourly engagement at $250 an hour to a full service at $15,000 + 5%.
Additional Resources
NAVAL AIR WARFARE CENTER AIRCRAFT DIVISIONAIR SYSTEMS GROUP, PROPULSION & POWER ENGINEERING BAA
Deadline: September 30th
Funding Award Size: Est. $500K to $5M
Description: Apply for FY26 Navy propulsion and power R&D funding through NAWCAD’s open BAA. Submit white papers by 30 September 2026 across energy, propulsion, and aircraft systems.
Below is a brief summary. Please check the full solicitation before applying (link in resources section).
Executive Summary:
This is a Fiscal Year 2026 Broad Agency Announcement (BAA) from the Naval Air Warfare Center Aircraft Division (NAWCAD) focused on propulsion and power technologies for future Naval aircraft. It is a rolling opportunity covering multiple technical areas (BAA 121–125) with a continuous submission window until 30 September 2026.
The Navy is actively seeking white papers and proposals across electrical power systems, fuels and lubricants, operational energy, maintenance/health monitoring, and propulsion systems. Awards are made on a rolling basis, and funding availability is uncertain—so early engagement is critical.
How much funding would I receive?
Number of Awards: Multiple awards anticipated
Estimated: $500K to $5 million. Award Size: Not predetermined; varies based on technical merit, relevance, and available funding
Period of Performance: Varies by project
Possible Award Instruments:
Procurement contracts
Grants
Cooperative agreements
Other Transaction (OT) agreements for research or prototypes
The Government reserves the right to fund all, some, or none of the submitted proposals and may fund efforts incrementally or with options.
What could I use the funding for?
Funding supports R&D programs aligned to five technical areas:
BAA 121: Advanced aircraft electrical power systems
BAA 122: Fuel and lubricant technology
BAA 123: Aircraft operational energy technology
BAA 124: Condition-based maintenance, diagnostics, and health monitoring
BAA 125: Advanced propulsion system technology
Across these areas, funding can be used for:
Concept feasibility studies
Modeling and simulation
Design and engineering
Prototype development
Testing and demonstration
Data analysis and validation
Programs are expected to include structured phases such as design, fabrication, and verification.
Are there any additional benefits I would receive?
Opportunity to transition technology into Navy aircraft systems
Potential for follow-on funding tied to program success
Direct alignment with Naval Air Systems Command priorities
Ability to structure proposals with optional components for incremental funding
Additional benefits are not explicitly specified beyond contract award and potential transition opportunities.
What is the timeline to apply and when would I receive funding?
Submission window: Open continuously until 30 September 2026
Process:
Step 1: Submit White Paper (≤30 pages)
Step 2: If invited, submit full technical and cost proposal
Expected award timing: Fiscal Years 2025–2029
Awards are made on a rolling basis depending on funding availability and program interest.
Where does this funding come from?
Naval Air Warfare Center Aircraft Division (NAWCAD)
Air Systems Group, Propulsion & Power Engineering Department
U.S. Navy / Naval Air Systems Command (NAVAIR)
Who is eligible to apply?
Eligible applicants include:
Private companies and contractors
Educational institutions
Small businesses and disadvantaged businesses
HBCUs and Minority Institutions
Veteran-owned and women-owned small businesses
Requirements:
Must meet Federal Acquisition Regulation (FAR) responsibility standards
Must be registered in SAM prior to award
Must have adequate accounting systems (for cost-reimbursable contracts)
Not eligible:
Foreign governments or foreign entities
What companies and projects are likely to win?
Proposals are evaluated primarily on:
Primary criteria (equal weight):
Scientific and technical merit
Relevance and contribution to Navy propulsion, power, and energy objectives
Secondary criteria:
Team capabilities and past performance
Cost realism and reasonableness
Winning projects will:
Align tightly with one of the defined BAA technical areas
Demonstrate clear military utility and transition potential
Show strong technical feasibility and ROI
Be ready for transition (especially for operational energy topics targeting near-term deployment)
Are there any restrictions I should know about?
Foreign entities are not allowed to apply
Organizational conflicts of interest must be disclosed and mitigated
SETA contractors cannot simultaneously perform R&D without approval
Subcontracting plans required for proposals over $700,000 (with small business participation goals)
Cost-reimbursable contracts require compliant accounting systems
Government is not obligated to provide requested equipment
Failure to disclose conflicts or meet requirements may result in rejection without evaluation.
How long will it take me to prepare an application?
White Papers are expected to be a few pages up to ~15 pages (max 30 pages)
Full proposals (if invited) require detailed technical and cost volumes
Preparation time is not explicitly specified, but the two-step process is designed to reduce upfront effort by screening via White Papers first.
How can BW&CO help?
BW&CO can:
Identify the strongest-fit technical area (BAA 121–125)
Develop a compliant and compelling White Paper
Position your technology for Navy transition and ROI
Build a full technical and cost proposal if invited
Structure optional work packages to maximize award likelihood
How much would BW&CO Charge?
Our full service support is available for a flat fee of $5,000 for the White Paper Submission.
Fractional support is $300 per hour, with most AFRL proposal projects requiring 10-20 hours of expert support from strategy through submission of full proposal.
For startups, we offer a discounted rate of $250 per hour to make top-tier grant consulting more accessible while maintaining the same level of strategic guidance and proposal quality.
Additional Resources
Review solicitation here.
CDMRP: Pancreatic Cancer Research Program (PCARP)
Deadline: TBD
Funding Award Size: $300k - $1.1m
Description: The FY26 Pancreatic Cancer Research Program (PCARP) offers up to $1.1M in total costs for early detection, translational research, and novel therapeutics. Pre-announcement released February 12, 2026.
Below is a brief summary. Please check the full solicitation before applying (link in resources section).
Executive Summary:
The FY26 Pancreatic Cancer Research Program (PCARP) is anticipated to issue multiple funding opportunities to accelerate impactful research in pancreatic cancer, spanning early detection, supportive care, risk characterization, access to care, metabolic dysregulation, tumor development, biomarkers, and new therapeutics. Investigators should begin planning now—formal Funding Opportunity Announcements (FOAs), deadlines, and application requirements will be posted on Grants.gov once released.
Pre-Applications are due on 7/07 and 9/16,
Full Applications are due on 10/07.
How much funding would I receive?
Funding varies by mechanism:
Focused Pilot Award: Up to $300,000 total costs over up to 2 years.
Idea Development Award: Up to $700,000 total costs over up to 3 years(standard) or $950,000 total costs with Partnering PI Option.
Translational Research Partnership Award: Up to $1.1 million total costs over up to 3 years.
What could I use the funding for?
Funding supports research that directly addresses one or more of the following PCARP Focus Areas:
Scientific & Clinical Focus Areas
Early detection research
Identification and characterization of risk
Supportive care, quality of life, and patient perspectives
Healthcare access barriers and care delivery challenges
Metabolic disruptions (including diabetes, cachexia)
Tumor development from precursor lesions to metastasis
Biomarkers for response prediction and management strategies
Novel therapeutic targets and approaches
Each award mechanism may have specific constraints on what types of work it can support (e.g., some do not fund clinical trials or basic research).
Are there any additional benefits I would receive?
Early insight into programmatic priorities via this pre-announcement.
Access to eBRAP system for managing pre-applications.
Email subscription updates when official FOAs are released.
What is the timeline to apply and when would I receive funding?
Focused Pilot Award
09-16-2026 - (Pre-application - Letter Of Intent)
10-07-2026 - (Application)
Idea Development Award
07-07-2026 - (Pre-application - Pre-Proposal)
10-07-2026 - (Application)
Translational Research Partnership Award
07-07-2026 - (Pre-application - Pre-Proposal)
10-07-2026 - (Application)
Where does this funding come from?
PCARP is funded through the FY26 Defense Appropriations Act and managed within the Defense Health Agency Research and Development – Medical Research and Development Command (DHA R&D-MRDC) as part of the Congressionally Directed Medical Research Programs (CDMRP).
Who is eligible to apply?
Eligibility depends on the award mechanism:
Focused Pilot Award: Investigators at any career level, including postdoctoral and clinical fellows.
Idea Development Award: Independent investigators at any career stage; early-career investigators may partner with experienced PIs.
Translational Research Partnership Award: Independent investigators; postdoctoral/clinical fellows are not eligible.
What companies and projects are likely to win?
Projects most competitive for PCARP will:
Directly address one or more specified focus areas with strong scientific rationale.
Demonstrate innovation and potential impact on pancreatic cancer outcomes.
Align with mechanism goals (e.g., pilot studies for early-stage ideas, partnerships for translational work).
Include appropriate preliminary data when required.
Are there any restrictions I should know about?
Focused Pilot Award: No basic research, pre-clinical animal studies, or clinical trials.
Idea Development & Translational Awards: Clinical trials and some animal work may be restricted or defined in FOA; check carefully.
Pre-proposal or letter of intent submission is required prior to full application for many mechanisms.
How long will it take me to prepare an application?
Time depends on mechanism and data readiness:
Focused Pilot Award: Plan ~4–8 weeks for a competitive pre-application and research plan.
Idea Development & Translational Awards: With required preliminary data, plan ~8–16+ weeks to assemble data, collaborators, and a strong proposal.
Start early given the expected complexity of CDMRP applications.
How can BW&CO help?
BW&CO can help you:
Interpret future FOA requirements and priorities.
Structure pre-applications/letters of intent for maximum impact.
Craft narrative, budget justification, and compliance sections.
Align scientific aims with program focus areas to increase competitiveness.
How much would BW&CO Charge?
We have both fractional engagements ($250 an hour) and full engagements ($13,000 + 5%) available.
Additional Resources
Review the solicitation here.
CDMRP: Lupus Research Program (LRP)
Deadline: TBD
Funding Award Size: $250k - $2m
Description: Apply for FY26 CDMRP Lupus Research Program funding. Awards up to $2M for lupus research, innovation, and quality-of-life studies.
Below is a brief summary. Please check the full solicitation before applying (link in resources section).
Executive Summary:
The CDMRP’s FY26 Lupus Research Program (LRP) pre-announcement signals anticipated funding opportunities supporting innovative, high-impact lupus research aimed at understanding, preventing, diagnosing, and treating lupus, as well as improving the quality of life for individuals living with lupus.
Pre-Applications are due on 7/29.
Full-Applications are due on 8/19.
How much funding would I receive?
The pre-announcement outlines multiple award mechanisms with specified maximum total costs:
Idea Award – up to $300,000 (2 years)
Impact Award – up to $1,000,000 (4 years)
Transformative Vision Development Award – up to $250,000 (2 years)
Transformative Vision Award – up to $2,000,000 (4 years)
What could I use the funding for?
Funding must support research aligned with one or more LRP focus areas:
Biological & Clinical Research
Mechanisms of lupus disease and pathobiology
Genetic, epigenetic, and gene–environment interaction studies
Disease heterogeneity, presentations, and outcomes
Applies to Idea & Impact Awards
Quality of Life & Intervention Studies
Addressing social determinants of health
Nutrition, symptom control, comparative effectiveness
Outcomes research and patient-reported outcomes
Applies to Impact, Transformative Vision Development, and Transformative Vision Awards
Innovative Health Care Delivery Models
Models improving lupus outcomes
Applies to Impact, Transformative Vision Development, and Transformative Vision Awards
Are there any additional benefits I would receive?
Mechanism clarity ahead of FOAs allows early planning.
Subscribe to email updates through eBRAP for timely notifications when FOAs are released.
Being positioned early can improve competitiveness.
What is the timeline to apply and when would I receive funding?
Pre-Applications are due on 7/29.
Full-Applications are due on 8/19.
Where does this funding come from?
Funding is provided through the FY26 Defense Appropriations Act appropriated to the Congressionally Directed Medical Research Programs (CDMRP) and managed by the Defense Health Agency Research & Development and Medical Research and Development Command (DHA R&D-MRDC).
Who is eligible to apply?
Eligibility is defined by mechanism:
Idea Award: Investigators at or above postdoctoral level.
Impact & Transformative Awards: Investigators at or above Assistant Professor (or equivalent).
Team Requirements: Transformative mechanisms must include at least one lupus consumer advocate as part of the research team.
What companies and projects are likely to win?
Projects that:
Align tightly with the specified focus areas.
Demonstrate high innovation and impact potential.
Involve strong preliminary data (as required for Transformative Vision Award).
Include meaningful involvement of lupus consumer advocates (for transformative mechanisms).
Are there any restrictions I should know about?
This pre-announcement is not a funding commitment; only the FOAs establish requirements and obligations.
Applications cannot support clinical trials in Idea or Impact Awards; Transformative Vision Awards may support clinical trials but not animal studies.
Transformative Vision Development Awards cannot support clinical trials or animal studies.
How long will it take me to prepare an application?
Preparation time depends on mechanism and complexity, but begin planning now — especially for pilot data and consumer engagement for transformative mechanisms. Historically, competitive CDMRP applications often require several weeks to months of focused preparation.
How can BW&CO help?
BW&CO can:
Develop alignment narratives tied to LRP focus areas.
Assist with preliminary data framing and research strategy articulation.
Craft strong consumer advocacy integration plans.
Ensure conformity with CDMRP review criteria once FOAs are released.
How much would BW&CO Charge?
We have both fractional engagements ($250 an hour) and full engagements ($13,000 + 5%) available.
Additional Resources
Review the solicitation here.
CDMRP: Breast Cancer Research Program (BCRP)
Deadline: TBD
Funding Award Size: $750k - $5m
Description: FY26 CDMRP Breast Cancer Research Program (BCRP) pre-announcement. Grants up to $35M for breakthrough, clinical, and consortium breast cancer research.
Below is a brief summary. Please check the full solicitation before applying (link in resources section).
Executive Summary:
The Breast Cancer Research Program (BCRP), managed by the Congressionally Directed Medical Research Programs (CDMRP), has released a Pre-Announcement for anticipated Fiscal Year 2026 (FY26) funding opportunities to support innovative, high-impact research aimed at ending breast cancer for Service Members, Veterans, their families, and the general public.
Deadlines for pre-applications range from 6/12 - 6/24. Full Applications range from 7/8 - 9/30.
How much funding would I receive?
The Pre-Announcement outlines anticipated award types with specified maximum total costs for FY26:
Breakthrough Award
Level 1: up to $750,000 (single PI) or $1.25M (partnering PIs)
Level 2: up to $1.65M (single PI) or $2.5M (partnering PIs)
Population Science (Level 2): up to $2.5M (single) or $3.35M (partnering)
Level 3: up to $5.6M (single) or $7M (partnering)
Level 4: up to $21M
(Breakthrough Awards range from early high-risk ideas to transformative approaches.)
Other Anticipated Mechanisms
Era of Hope Scholar Award: up to $4.9M
Clinical Research Extension Award: up to $7M (single) / $8.4M (partnering)
Transformative Breast Cancer Consortium Award: up to $35M
Transformative Breast Cancer Consortium Development Award: up to $140,000
(These awards support early-career investigators, ongoing clinical research, and large multi-project consortia.)
What could I use the funding for?
Funded research must address one or more overarching challenges critical to ending breast cancer:
Topic Areas / Research Aims
Primary prevention of breast cancer
Determinants of initiation, risk, or susceptibility
Distinguishing lethal vs. non-lethal tumors
Solutions to overdiagnosis/overtreatment
Pathways driving tumor growth and metastasis
Mechanisms of dormancy and lethal recurrence
More effective, less toxic treatments
Reducing mortality from metastatic disease
Mechanism-Specific Uses
Breakthrough Awards: high-risk/high-reward or translation-focused research
Era of Hope Scholar Award: early-career leadership and innovation
Clinical Research Extension: extending clinical data collection and analysis
Consortium Awards: integrated multi-project collaborations toward transformative goals
(Mechanism scopes will be confirmed in the FOAs.)
Are there any additional benefits I would receive?
Participating teams may benefit from:
Collaborative frameworks with consumer advocates required on some mechanisms
Access to eBRAP support and templates for submission guidance
What is the timeline to apply and when would I receive funding?
Breakthrough Award - Funding Level 1
06-24-2026 - (Pre-application - Letter Of Intent)
07-08-2026 - (Application)
Breakthrough Award Level 3
06-12-2026 - (Pre-application - Pre-Proposal)
09-30-2026 - (Application)
Breakthrough Award Level 4
06-12-2026 - (Pre-application - Pre-Proposal)
09-30-2026 - (Application)
Clinical Research Extension Award
06-24-2026 - (Pre-application - Letter Of Intent)
07-08-2026 - (Application)
Era of Hope Scholar Award
06-24-2026 - (Pre-application - Letter Of Intent)
07-08-2026 - (Application)
Transformative Breast Cancer Consortium Award
06-12-2026 - (Pre-application - Pre-Proposal)
09-30-2026 - (Application)
Transformative Breast Cancer Consortium Development Award
06-24-2026 - (Pre-application - Letter Of Intent)
07-08-2026 - (Application)
Where does this funding come from?
This funding is provided by the FY26 Defense Appropriations Act under the Department of Defense’s Congressionally Directed Medical Research Programs, specifically appropriated for breast cancer research.
Who is eligible to apply?
Eligibility varies by mechanism but generally includes:
Investigators at all academic levels or equivalent (Breakthrough, Clinical Extension)
Independent investigators (higher level awards)
Teams including consumer advocates for specified awards
Exact eligibility will be detailed in each FOA.
(Final eligibility criteria are determined in the FOAs.)
What companies and projects are likely to win?
Competitive proposals typically:
Address key overarching challenges defined by BCRP
Demonstrate innovation, clinical relevance, and impact
Include translational pathways or transformative potential
Meet mechanism-specific expectations (e.g., data access plans, interdisciplinary teams)
Are there any restrictions I should know about?
This pre-announcement is not a FOA and does not guarantee funding.
Final applications must conform to Grants.gov FOAs once released.
Mechanism specific limits on clinical trials and preliminary data requirements will be in each FOA.
How long will it take me to prepare an application?
Preparation time varies by project complexity, but given the breadth of mechanisms and expected competitive standards, begin planning now while awaiting FOAs:
Concept refinement: ~2–4 weeks
Team assembly & consumer advocate engagement: ~2–6 weeks
Budget & prelim data planning: ~4–8+ weeks depending on scope
How can BW&CO help?
BW&CO can assist with:
Translating BCRP FOA language into tailored project responses
Drafting narrative, budget justification, and impact sections
Aligning your concept with mechanism-specific review criteria
Incorporating consumer review perspectives where required
How much would BW&CO Charge?
We have both fractional engagements ($250 an hour) and full engagements ($13,000 + 5%) available.
Additional Resources
Review the solicitation here.