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Small Businesses: Review important information about NIH’s foreign disclosure requirement (last updated 05/20/2025) is sponsored by National Institutes of Health (NIH). Innovation/small business research opportunity from National Institutes of Health (NIH): Small Businesses: Review important information about NIH’s foreign disclosure requirement (last updated 05/20/2025).
This opportunity supports small business innovation and technology development. Visit the agency page for full solicitation details and application instructions.
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Or search similar grants →According to the current listing, eligibility includes: Small business concerns (SBCs) organized for profit, with a place of business in the United States; at least 51% owned and controlled by one or more U.S. citizens or permanent residents; no more than 500 employees including affiliates. Principal investigator must be primarily employed by the SBC (SBIR) or the research institution (STTR). Confirm the full requirements in the official notice before applying.
Yes — Small Businesses: Review important information about NIH’s foreign disclosure requirement (last updated 05/20/2025) is offered by National Institutes of Health (NIH) and this listing comes from SBIR, an official U.S. federal source. Federal applications generally require registrations (for example SAM.gov or an agency submission portal), so allow extra lead time.
Start from the official opportunity page linked in this listing — it carries the sponsor's submission instructions.
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.
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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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