№ files_lp_3_process_7_090736
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This document is a request for information aimed at gathering data from potential industry partners capable of manufacturing and testing the Army Liposome Formulation-QS21 (ALFQ) under cGMP conditions for clinical trials and future commercial use.
Agency: U.S. Army Medical Materiel Development Activity (USAMMDA)
Location: 1430 Veterans Drive, Ft. Detrick, MD 21702
NAICS: 541715 (Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology))
PSC: AN13 (Health R&D Services; Health care services; Experimental Development)
Subject: The USAMMDA is conducting market research to determine whether a commercial solution can be provided to meet requirements for cGMP manufacturing of a minimum of 20,000 vials/lot of vials of the Army Liposome Formulation-QS21 (ALFQ) for Phase 2/3 clinical trials and the capability to manufacture for a commercially licensed vaccine. This market research may also assist with the further development and/or refinement of the requirements.
Description: USAMMDA has a requirement to manufacture and release a minimum of 20,000 vials/lot of ALFQ under cGMP.
Year: 2026
Region / City: Ft. Detrick, MD
Topic: cGMP manufacturing, liposome formulation, vaccine production
Document Type: RFI (Request for Information)
Organization: U.S. Army Medical Materiel Development Activity (USAMMDA)
Author: U.S. Army
Target Audience: Industry partners, manufacturers of pharmaceutical products
Period of Validity: N/A
Approval Date: N/A
Amendment Date: N/A
Price: 8 / 10 USD
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