Requirement for supply of Freeze Dried Plasma (FDP) product available under a Food and Drug Administration (FDA) authorized Emergency Use Authorization (EUA)

SOL #: HT9427-26-NOI-TJK1Special NoticeSole Source

Overview

Buyer

DEPT OF DEFENSE
Defense Health Agency (Dha)
DEFENSE HEALTH AGENCY
FORT DETRICK, MD, 21702, United States

Place of Performance

MD

NAICS

Research and Development in the Physical (541715)

PSC

Pharmacy Services (Q517)

Set Aside

No set aside specified

Timeline

1
Posted
Apr 2, 2026
2
Action Date
Apr 17, 2026, 4:15 PM

Qualification Details

Fit reasons
  • NAICS alignment with historical contract wins in similar service areas.
  • Scope strongly matches core technical capabilities and delivery model.
Risks
  • Past performance thresholds may require one additional teaming partner.
  • Potential clarification needed on staffing minimums before bid/no-bid.
Next steps

Validate eligibility requirements, assign capture owner, and schedule partner outreach to confirm teaming strategy before submission planning.

Quick Summary

The Department of Defense (DEPT OF DEFENSE), specifically the Defense Health Agency (DHA), has issued a Special Notice regarding a critical requirement for the supply of Freeze Dried Plasma (FDP) product available under a Food and Drug Administration (FDA) authorized Emergency Use Authorization (EUA). An expanded supply contract is anticipated to be issued on a sole-source basis. Responses from interested parties are due by April 17, 2026.

Scope of Work

This requirement is for the provision of Freeze Dried Plasma (FDP) product that is authorized for use under an FDA Emergency Use Authorization (EUA). The government has identified a critical need for this product.

Contract & Timeline

  • Type: Special Notice (anticipates sole-source contract)
  • NAICS Code: 541715 (Research and Development in the Physical, Engineering, and Life Sciences (except Biotechnology))
  • Size Standard: 1,000 employees
  • Set-Aside: None specified
  • Response Due: April 17, 2026, 4:15 PM ET
  • Published: April 2, 2026, 6:48 PM ET
  • Place of Performance: Maryland (MD), Postal Code 21702, United States

Evaluation

This notice is to identify any sources that believe they are eligible to provide the required FDP product under an EUA. Responses must be submitted in writing and supported with clear and convincing evidence articulating the ability to meet this requirement. A request for documentation alone will not be considered an affirmative response.

Additional Notes

This is a market research effort to confirm the sole-source determination. The government will review responses to determine if other qualified sources exist.

People

Points of Contact

Files

Files

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Versions

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Special Notice
Posted: Apr 2, 2026
Requirement for supply of Freeze Dried Plasma (FDP) product available under a Food and Drug Administration (FDA) authorized Emergency Use Authorization (EUA) | GovScope