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NSF 26-510 | Medical Devices — Procedural Technologies or Visualization

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nsf-seedfund-MD-MD6_STTRSBIR / STTR

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Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.

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The National Science Foundation is soliciting proposals under the Medical Devices program, specifically focusing on Procedural Technologies or Visualization. This initiative seeks leading edge innovations that introduce new medical technologies or translate emerging scientific principles into health practice. The program is designed to support the development of novel device platforms based on new discoveries or scientific approaches. This is a total small business set-aside under the SBIR/STTR mandate for companies with fewer than 500 employees. While limited human subject studies for feasibility or proof-of-concept are permitted, the program strictly prohibits proposals for clinical trials intended to demonstrate safety and efficacy, sample size calculations, or work performed for regulatory purposes and post market surveillance. Noncompliant proposals requesting support for clinical trials will be returned without review.

General Info

NSF SBIR/STTR set-aside for innovative medical device platforms; clinical trials are prohibited.

Agency

National Science FoundationView Agency

NAICS

541715 - Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)View NAICS

Place of Performance

Not specified

Set-Aside

SBA

Documents

(0)

No documents available

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PhaseSolicitation
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Solicitation

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Organization & Contact Information

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AgencyNational Science Foundation
ContactsNo contacts available
OfficeUSA
Organization / Agency
National Science Foundation
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Office AddressUSA
ContactsNo contact information available

Full Description

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The Medical Devices topic aims to develop novel medical device platforms, introduce innovative medical technologies or translate emerging scientific principles into health practice. Proposals should be considered leading edge innovations, typically based on a discovery, new approach or new scientific principle to medical devices or technologies. Limited human subject clinical studies may be acceptable if they are performed in support of feasibility or proof-of-concept objectives. The program does not support proposals to conduct clinical trials for sample size calculations, statistically demonstrate safety or efficacy or the development of pre-clinical or clinical-stage drug candidates. Clinical work performed primarily for regulatory purposes or post market surveillance are also not allowed. Proposals requesting support for clinical trials are noncompliant with the SBIR/STTR solicitation and returned without review.
## Subtopic: Procedural Technologies or Visualization

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