FDA/CDRH Scientific Technical Capacity for Regulatory Review

AI Summary: The FDA's Center for Devices and Radiological Health (CDRH) seeks expert scientific and technical consultants to support regulatory review of medical devices across their total product lifecycle, including activities such as 510(k) and PMA application reviews, cybersecurity consultations, regulatory auditing, and research. The work will be performed in Silver Spring, Maryland, with consultants needed across diverse specialties including biomedical engineering, statistics, software engineering, toxicology, cardiology, and numerous other scientific and clinical disciplines. This is a sources sought notice with no set-aside, and the engagement will be structured as a Blanket Purchase Agreement with call orders for specific projects.

Opportunity Details

Solicitation Number: 75F40127Q00006

Date Added: October 31, 2026

Description:

https://api.sam.gov/prod/opportunities/v1/noticedesc?noticeid=a44805a9ad5c402992f8d6e74c90cd28

Set-Aside: No Set aside used (NONE)

Place of Performance: Silver Spring, Maryland, UNITED STATES

NAICS Codes:
541611

Files:

FDA/CDRH Scientific Technical Capacity for Regulatory Review

Opportunity Details

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