No attachments available.
Freeze Dried Plasma (FDP) Emergency Use Authorization or FDA Licensed Product
Contact and place of performance
Timothy Kelly
MD 21702
USA
Dept of Defense - Operational Medicine (OPMED) is seeking to procure either a Food and Drug Administration (FDA) licensed Freeze Dried Plasma product or a Freeze Dried Plasma product that has a current Emergency Use Authorization (EUA) from the FDA. OPMED is seeking potential industry partners who have a FDP product at this stage of development.
The Defense Health Agency (DHA) issued this sources sought notice, solicitation number HT9427-26-RFI-704, on behalf of the Department of Defense Operational Medicine (OPMED). OPMED intends to identify potential industry partners capable of providing Freeze Dried Plasma (FDP) products that are either Food and Drug Administration (FDA) licensed or currently hold an FDA Emergency Use Authorization (EUA). This market research focuses on identifying vendors who have reached these specific regulatory stages of development for FDP products.
The procurement is classified under NAICS code 325414, Biological Product (except Diagnostic) Manufacturing, and PSC 6515, Medical and Surgical Instruments, Equipment, and Supplies. There is no set-aside designated for this requirement. Performance is cited to take place in Maryland, and Timothy Kelly is the designated point of contact.
Responses to this notice are due by March 25, 2026. The original notice was published on March 9, 2026, and updated on March 10, 2026. At the time of publication, there are zero attachments associated with this solicitation on SAM.gov.
Generated by Lumen AI
Scoped analysis and attachments—go beyond the summary when you need detail from the solicitation package.