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NSF 26-510 | Biomedical Technologies — Monitoring Devices

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nsf-seedfund-BM-BM5_SBIRSBIR / STTR

Contract Overview

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The National Science Foundation is soliciting proposals under the Biomedical Technologies program, specifically focusing on Monitoring Devices through the nsf-seedfund-BM-BM5_SBIR solicitation. This initiative supports the early-stage development of innovative products, processes, or services designed to improve the quality and economic efficiency of healthcare. The opportunity is a total small business set-aside, restricted to organizations with fewer than 500 employees. Funding is intended for early-stage technological development and feasibility studies, including limited proof-of-concept work with human subjects. However, the program strictly prohibits the use of funds for clinical trials, safety or efficacy studies, the development of pre-clinical or clinical-stage drug candidates and medical devices, or activities primarily intended for regulatory purposes. Proposals requesting support for clinical studies will be considered noncompliant and returned without review.

General Info

NSF SBIR funding for small businesses developing innovative healthcare monitoring devices and technologies.

Agency

National Science FoundationView Agency

NAICS

334510 - Electromedical and Electrotherapeutic Apparatus ManufacturingView NAICS

Place of Performance

Not specified

Set-Aside

SBA

Documents

(0)

No documents available

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Timeline

PhaseSolicitation
Posted

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 Biomedical Technologies topic aims to support the early-stage development of novel products, processes or services that will enable the delivery of high-quality, economically efficient healthcare. Subtopics are not aimed at supporting or conducting clinical trials, clinical efficacy or safety studies, the development pre-clinical or clinical-stage drug candidates or medical devices, or work performed primarily for regulatory purposes. Limited studies with human subjects may be acceptable to the extent that they are performed in support of feasibility, such as proof-of-concept studies of early-stage technologies. Proposals that request support for clinical studies will be deemed noncompliant with the SBIR/STTR solicitations and returned without review.
## Subtopic: Monitoring Devices

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