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Biomedical & Pharmaceutical R&D

Active
Federal

Contract Overview

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

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This subcontract under the Defense Health Agency for the Department of Defense focuses on biomedical and pharmaceutical research and development. The primary objective is to support prime contractors on USSOCOM projects by developing drug and biologic formulations, conducting efficacy and biocompatibility analyses, and performing stability testing. A critical goal of this work is to eliminate the need for refrigeration and cold-chain requirements to ensure these medical compounds are viable for field use. The scope of work requires the delivery of validated drug or biologic compounds and comprehensive clinical trial data. Classified under NAICS code 541715, the opportunity was posted on July 29, 2026, with a response deadline of August 1, 2028.

General Info

DHA subcontract for non-refrigerated biomedical and pharmaceutical R&D supporting USSOCOM projects.

NAICS

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

Place of Performance

MD

Set-Aside

NONE

Documents

This scope was carved out of HT9425-23-S-SOC1-0003.

The full solicitation package (5 documents), including the RFP, is on the prime solicitation, not on this scope.

View the prime solicitation

BROAD AGENCY ANNOUNCEMENT (BAA) for Extramural Biomedical and Human Performance Research and Development - HT9425-23-S-SOC1

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Timeline

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Organization & Contact Information

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AgencyDepartment Of Defense → Defense Health Agency
ContactsNo contacts available
OfficeN/A
Office AddressN/A
ContactsNo contact information available

Full Description

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Performs research and development of drugs or biologics for prime contractors on USSOCOM biomedical projects. Develops formulations, conducts efficacy and biocompatibility analysis, and performs stability testing to eliminate refrigeration and cold-chain requirements for field use. Delivers validated drug/biologic compounds or clinical trial data.

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