Non-Dilutive Funding Program
High interest focus areas include, but are not limited to:
- Advanced Assays and Reagents for omics, cell-based, and imaging applications to speed up medical countermeasure development
- Drug Candidate Identification Technologies (including in silico models) that can identify new or repurposed candidates that address health security threats
- AI-Based Tools/Algorithms and Automation to develop predictive analytics and/or model process parameters to expedite biopharmaceutical manufacturing of medical countermeasures
- Novel Sample Prep, Automation, or Miniaturization Tools to speed up development of medical countermeasures and biomanufacturing capabilities
- Analytical Platforms applicable to multiple Vaccines/Therapeutic Products with a focus on rapid Critical Quality Assurance analytical testing technologies for Drug Substances and Drug Products to harmonize release assays and potency assays
- Digital Twin Approaches using Multimodal Clinical Data, including AI (e.g., EHR, imaging, unstructured notes) to enable early identification, endotyping, or treatment guidance for disease severity to enable early intervention
- Integrated Bioprocess Optimization combined with modeling to establish control strategy and expedite manufacturing of medical countermeasures
- Novel Approaches for Generation of Polyclonal Recombinant Antibodies to treat infectious diseases
For more information on BARDA areas of interest, visit https://drive.hhs.gov/partner.html. You may also find BARDA’s strategic priorities by visiting the pages for each of BARDA’s medical countermeasure programs: https://medicalcountermeasures.gov/
BARDA also recently released TPPs relevant to some of its areas of interest: https://medicalcountermeasures.gov/barda/tpp.
We are accepting proposals from early-stage biotech companies as well as academic and other innovators globally.
We are accepting proposals from early-stage biotech companies as well as academic and other innovators globally. Companies and individuals are welcome to submit an application for the Accelerator Program and a proposal for non-dilutive (DEV) funding from BTI VANGUARD. Applications and proposals will be reviewed independently. Solicitations for both the Accelerator Program and non-dilutive (DEV) funding opportunities will be open on an annual basis.
No, SAM.gov registration is not required.
- Preliminary Proposal Deadline: September 30, 2025
- Invitation to Submit Full Proposal: By November 15, 2025
- Program Start: March 2026
Proposals will be evaluated with a particular focus on 1) the ability of the technology in the proposal to support BARDA’s mission, 2) the uniqueness of the innovation and its ability to address unmet needs, and 3) the capacity for the proposed use of funds to advance the technology to the next value inflection point.
It is anticipated that project milestones will be completed in 6 months from the start of the project, and that the funding will be spent during this time period. Project management and mentor support will be provided during this 6-month period. BTI VANGUARD and BARDA also understand that unforeseen and unpredicted events happen during development, evaluation and validation activities.
There will be reporting requirements on a monthly basis, upon milestone achievement, a mid-project meeting with BARDA, and a final report and presentation.
Allowable expenses for the non-dilutive funds from BTI VANGUARD include: direct costs for development, evaluation, or validation activities, and labor for personnel and subcontractors/CRO partners contributing to the milestone completion. We recommend that the budget is well-distributed across expense categories (e.g. not spending the full budget on a piece of equipment) and keeping personnel costs below 60%.
Companies and individuals that receive funding from BTI VANGUARD will have access to BARDA subject matter experts and other related BARDA resources. Access to these BARDA resources will be managed and coordinated by the BTI VANGUARD Team.
A technology that aligns to the BTI VANGUARD Hub might also be aligned to some of the other BAN Hubs, including Therapeutics/Vaccines and Diagnostics/Medical Devices. Organizations should also look into open Areas of Interest for the BARDA DRIVe EZ-BAA funding opportunity and other BARDA funding and partnership opportunities. The decision about which Hub or program to apply to is up to the organization.
- BARDA DRIVe: https://drive.hhs.gov/partner.html
- BARDA BAA funding: https://medicalcountermeasures.gov/barda/barda-baa/
- BARDA’s main page: www.medicalcountermeasures.gov
ReadyDetect: Blood Sampling Competition
General Overview
ReadyDetect is a $5 million prize competition focused on advancing next-generation blood sample collection and processing devices for use in decentralized settings, including the home, field, and resource-limited environments.
The competition consists of two stages:
- Stage I (Concept): Concept paper submission
- Stage II (Prototype): Completion report & data submission detailing prototype development, testing, and validation
Up to eight winners will be selected across both stages.
No. The two stages are independent. Applicants may apply to either stage or both, depending on their level of development.
Eligibility & Teaming
Commercial, academic, and non-profit organizations are eligible. Academic and non-profit entities must partner with a commercial entity.
Yes. The primary entrant must be a U.S.-based entity at the time of submission and through prize award.
Yes. Teams may include subcontractors, consultants, CROs, and partners. The primary entrant must lead the technical effort.
Yes, provided each submission represents a distinct technology or approach.
Concept Stage (Stage I)
Applicants must submit a concept paper (maximum 10 pages) describing their innovation, development plan, and approach to prototype development and validation.
Yes. Submissions must include quantitative preliminary data and a Technology Readiness Level (TRL).
No specific TRL is required. Applicants at all stages are encouraged to apply, but must provide sufficient technical justification and supporting data.
No. The Concept Stage is not funded upfront. Up to five winners are selected after evaluation and each will receive a $100,000 prize.
No. To ensure fairness, feedback will not be provided between stages.
Prototype Stage (Stage II)
Applicants must submit a letter of intent and required regulatory documentation, including a clinical collection protocol, informed consent forms, and IRB approval or exemption.
Entrants must develop and test a functional prototype, conduct human subject testing (N≥75), and submit a final report with supporting experimental data demonstrating device performance, usability, and diagnostic compatibility.
Prototype Stage prizes are awarded after completion of the prototype work and evaluation of final submissions. Prizes are expected to be awarded in the summer of 2028.
No. The Prototype Stage is not funded upfront. Up to three winners are selected after evaluation and each will receive a $1,500,000 prize.
Yes. Prototype Stage submissions may be reviewed as they are received, and winners may be selected on a rolling basis.
Technical Requirements
Devices that enable self- or caregiver-administered blood collection, support plasma and/or serum separation, and integrate with antigen or molecular diagnostic tests.
No. FDA approval is not required at the prototype stage. However, applicants should demonstrate a clear path toward regulatory approval as part of future development.
Yes. Devices must be compatible with at least one antigen or molecular diagnostic test, preferably FDA-cleared.
Yes. Prototype Stage submissions must include data from at least 75 human subjects, including both pediatric and adult populations.
Yes. Applicants must provide a Cost of Goods (COGs) analysis at a 100,000-unit manufacturing scale, supported by vendor quotes.
Cost targets are intentionally ambitious to encourage breakthrough innovation. Applicants should provide well-supported assumptions and justification.
Intellectual Property & Confidentiality
Entrants retain ownership of their intellectual property. Applicants must demonstrate access to all IP required to develop and commercialize their solution.
Submissions will be reviewed by authorized evaluators. Non-confidential information about selected winners may be publicly disclosed, with appropriate review.
Submission Process
Applications are submitted through an online portal that guides applicants through each required component.
Yes. Applications can be modified up through the deadline.
Late submissions will not be accepted.
Yes, but it must be clearly identified at the sentence level.
Additional Questions
Yes. Virtual information sessions will be held during both stages. Please see the timeline on the main webpage for the dates and links to register.
Please refer to the PHEMCE Priority Threats List.
For additional information, please contact: ReadyDetect@biotoolsinnovator.org.
Level UP-XR Program
Control groups may be real-time cohorts or utilize historical training data or retrospective benchmarks.
You are NOT required to have a partner at the onset. Applicants may apply individually during the preliminary proposal phase. Those without a pre-designated partner will be matched with possible synergistic partners. Selection of partners will need to be completed in order for the pairing to submit a full proposal.
For this pilot program, this is used to capture augmented reality (AR) and virtual reality (VR) platforms.
Each pair may propose a combined budget amount up to $300,000. The full proposal will outline who will receive the sub-award amounts and for what activities or reasons.
For additional information and questions, please contact vanguard@biotoolsinnovator.org.