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Research Evaluation and Commercialization Hubs (REACH) Program is sponsored by National Institutes of Health (NIH). The REACH program supports academic innovators in converting scientific discoveries into medical products and trains a diverse biomedical workforce in technology development and entrepreneurship. It provides education, training, funding tied to milestones, and expert feedback for product development.
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Or search similar grants →According to the current listing, eligibility includes: Academic innovators. Hubs leverage state government resources, local academic institutions, and industry partners. Confirm the full requirements in the official notice before applying.
The current listing shows NIH committed $1 million per year for four years to five new REACH hubs in 2023. Verify award ceilings, matching requirements, and allowable costs in the official notice.
Research Evaluation and Commercialization Hubs (REACH) Program is funded by National Institutes of Health (NIH). Verify program details on the funder's official page before applying.
Start from the official opportunity page linked in this listing — it carries the sponsor's submission instructions.
Past winners and funding trends for this program
PA-27-037 consolidates the Predoctoral to Postdoctoral Transition Award into a single parent announcement across 20 NIH components, with the next deadline December 8, 2026. The eligibility gate is not the science — it is a mandatory change of institution and mentor between the F99 and K00 phases.
Read articleA draft executive order would have put OMB Director Russell Vought on a commission with final say over NIH awards after peer review. Sen. Collins killed it by pointing at a provision Congress already passed. Here is what the episode teaches applicants about the December 11 cliff.
Read articlePA-27-034, PA-27-035 and PA-27-036 replace the institute-specific R25 announcements that research education programs have been built around for a decade. NCI, NIDA and NIGMS have already expired theirs early. Here is what the consolidation actually changes: an 8% indirect cost ceiling, a US-citizens-and-permanent-residents participant rule, a cooperative agreement variant that only exists on one of the three, and no clinical-trial-allowed companion anywhere.
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