The short answer. SBIR and STTR authority lapsed on October 1, 2025 and was restored by Public Law 119-83, approved April 13, 2026, through September 30, 2031. NIH Phase I awards go up to $323,090 and Phase II up to $2,153,927 under SBA guidelines. The next NIH standard due date is January 5, 2027; the next NSF full proposal deadline is November 4, 2026.

What happened in 2025 and 2026

NIH in 2026 and 2027

ItemFigure
Phase I (SBA guideline)$323,090
Phase II (SBA guideline)$2,153,927
Commercialization Readiness Pilot$4,191,495, up to 3 years
Standard due dates (PA-27-100)September 5, 2026; January 5, 2027; April 5, 2027
Applications per companyUp to 9 new and resubmitted Phase I, Fast-Track and Direct to Phase II applications per fiscal year
Late applicationsNot accepted
Some institutes allow larger budgets (up to $700,000 for Phase I and $3,000,000 for Phase II); NIBIB, NIAMS and NIDCR follow the SBA guideline in PA-27-100.

For device companies, NIBIB lists interest in bionics, medical devices, medical simulators, robotics, imaging and point-of-care technologies. It accepts Commercialization Readiness Pilot projects but not Phase IIB. Fast-Track lets you apply for Phase I and Phase II in one application.

NSF

ItemFigure
Phase IUp to $305,000, 6 to 18 months
Phase IIUp to $1,250,000, typically 24 months
Next full proposal deadlinesNovember 4, 2026; March 4, 2027; July 7, 2027
First stepAn invited Project Pitch; at most two pitches per company per 12 months

How much work can go to an outside engineering firm

Program and phaseMinimum done by the small businessThird parties
SBIR Phase ITwo thirds (67%) of the research effortGenerally not more than 33%
SBIR Phase IIOne half (50%)Up to 50%
STTRAt least 40%At least 30% by one partner research institution
NIH PA-27-100 and PA-27-102; SBA Policy Directive, May 3, 2023. SBIR deviations need written approval from the grants management officer; STTR deviations are not allowed.

PA-27-100 also states that applications involving foreign subawards or subcontracts will be deemed noncompliant. If grant money will pay for outside engineering, confirm where the work will be performed and which legal entity performs it with your program officer before you name a partner in the application.

Planning tips

Lisa Voronkova talked about the risks that sink medical device products on the Grant Engine roundtable.

Sources

What OVA does here, and where our responsibility ends

OVA Solutions is a medical device engineering group working under an ISO 13485:2016 certified quality system: 62 engineers, 220 devices developed, $125 per hour, offices in New York, Florida, the United Kingdom, Estonia and Ukraine. We design electronics, firmware and mechanics and take a device from concept to design for manufacturing. We are not a regulatory consultancy and not a contract manufacturer: the regulatory strategy and the submission stay with you or your regulatory consultant.

More from OVA: what medical device development costs, how to choose a development firm, answers from Lisa Voronkova, our quality system.

Updated on October 8, 2026.