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CBRN Medical Countermeasure (MCM) Candidate Developer

Open

Federal

Contract Overview

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

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This subcontract with the Department of Defense focuses on the development of medical countermeasure candidates for prime contractors on CPE CBRND projects. The scope of work includes conducting in vitro and in vivo efficacy testing, generating data through validated animal models, and managing FDA sponsor engagements and IND status. The developer is responsible for executing Phase I, II, and III clinical trials to deliver a licensed or advanced-stage medical countermeasure product. To ensure regulatory success, the contractor must possess significant FDA regulatory expertise and maintain strict compliance with GLP and GMP standards. This effort falls under NAICS code 541714 and is managed by the W6QK Acc-Apg agency.

General Info

DoD subcontract for developing medical countermeasures through clinical trials and FDA regulatory compliance.

Agency

Department Of Defense → W6QK Acc-Apg

NAICS

541714 - Research and Development in Biotechnology (except Nanobiotechnology)

Place of Performance

MD

Set-Aside

NONE

Documents

This scope was carved out of W911SR-26-R-HEAL.

The full solicitation package (4 documents), including the RFP, is on the prime solicitation, not on this scope.

View the prime solicitation

Chemical, Biological, Radiological, and Nuclear (CBRN) Medical Countermeasure (MCM) Participant Basic Agreement (PBA)

AI Contract Breakdown

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Timeline

PostedAug 19

subcontract

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Organization & Contact Information

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AgencyDepartment Of Defense → W6QK Acc-Apg

ContactsNo contacts available

OfficeN/A

Organization / AgencyDepartment Of Defense → W6QK Acc-Apg

Office AddressN/A

ContactsNo contact information available

Full Description

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Develops medical countermeasure candidates for prime contractors on CPE CBRND projects. Conducts in vivo and in vitro efficacy testing, generates data in validated animal models, manages FDA sponsor engagements and IND status, and executes Phase I, II, and III clinical trials. Requires GLP and GMP compliance and FDA regulatory expertise. Delivers a licensed or advanced-stage medical countermeasure product.

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