Freeze Dried Plasma (FDP) Emergency Use Authorization or FDA Licensed Product HT9427-26-RFI-704
Summary
AI-generated · Mar 10, 2026Freeze Dried Plasma (FDP) product is being sought with two acceptable regulatory statuses: FDA-licensed or a FDP product that currently holds FDA Emergency Use Authorization (EUA). The effort aims to identify potential industry partners who already have an FDP product at this development stage and could supply for operational medical use.
This is a sources-sought inquiry to gauge market availability and capability; the government is looking for manufacturers or developers with an FDP product that meets either regulatory status.
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.
From Sources Sought posted on Mar 09, 2026Dept 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.
From Sources Sought posted on Mar 10, 2026Notice history
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Sources Sought LATEST Posted Mar 10, 2026View changes (1)
- Response Deadline: Mar 13, 2026 → Mar 25, 2026
Details
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Contacts
Agency
Place of Performance
USA