Freeze Dried Plasma (FDP) Emergency Use Authorization or FDA Licensed Product

Agency: DEPT OF DEFENSE
State: Maryland
Type of Government: Federal
FSC Category:
  • 65 - Medical, Dental, and Veterinary Equipment and Supplies
NAICS Category:
  • 325414 - Biological Product (except Diagnostic) Manufacturing
Set Aside: No Set aside used
Posted Date: Mar 9, 2026
Due Date: Mar 13, 2026
Solicitation No: HT9427-26-RFI-704
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Contact information: Please Login to View Page
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Description

Follow
Freeze Dried Plasma (FDP) Emergency Use Authorization or FDA Licensed Product
Active
Contract Opportunity
Notice ID
HT9427-26-RFI-704
Related Notice
Department/Ind. Agency
DEPT OF DEFENSE
Sub-tier
DEFENSE HEALTH AGENCY (DHA)
Office
DEFENSE HEALTH AGENCY
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General Information
  • Contract Opportunity Type: Sources Sought (Original)
  • Original Published Date: Mar 09, 2026 11:08 am EDT
  • Original Response Date: Mar 13, 2026 12:15 pm EDT
  • Inactive Policy: 15 days after response date
  • Original Inactive Date: Mar 28, 2026
  • Initiative:
    • None
Classification
  • Original Set Aside: No Set aside used
  • Product Service Code: 6515 - MEDICAL AND SURGICAL INSTRUMENTS, EQUIPMENT, AND SUPPLIES
  • NAICS Code:
    • 325414 - Biological Product (except Diagnostic) Manufacturing
  • Place of Performance:
    MD 21702
    USA
Description

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.


Attachments/Links
Contact Information
Contracting Office Address
  • MEDICAL R & D CONTRACTING DIVISION 2 808 SCHREIDER STREET
  • FORT DETRICK , MD 21702
  • USA
Primary Point of Contact
Secondary Point of Contact


History
  • Mar 09, 2026 11:08 am EDTSources Sought (Original)

Related Document

Mar 11, 2026[Sources Sought (Updated)] Freeze Dried Plasma (FDP) Emergency Use Authorization or FDA Licensed Product
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