Question 1

What is "Freeze Dried Plasma (FDP) Emergency Use Authorization or FDA Licensed Product"?

Accepted Answer

**PROCUREMENT OVERVIEW:**  
The Defense Health Agency (DHA) is seeking proposals for the procurement of Freeze Dried Plasma (FDP) intended for emergency use authorization or as an FDA-licensed product. The core objective is to enhance the medical capabilities of the Department of Defense by providing a critical blood product that can be utilized in trauma care and emergency situations, particularly for military personnel in combat or disaster scenarios. The project aims to ensure the availability of FDP to meet urgent medical needs.

**ISSUING ORGANIZATION:**  
The issuing organization is the Defense Health Agency (DHA), located in Maryland, USA. The primary contact for this opportunity is Timothy Kelly, who can be reached at timothy.j.kelly169.civ@health.mil.

**KEY DATES:**  
- Posted Date: March 10, 2026  
- Proposal Due Date: March 25, 2026  
- Anticipated Award Date: Not specified  
- Performance Period: Not specified

**CONTRACT DETAILS:**  
The contract type is not explicitly stated in the provided information. There is no mention of an estimated contract value or budget range. Additionally, no option years are indicated.

**MANDATORY REQUIREMENTS:**  
Bidders must meet the following eligibility criteria:  
- Required certifications and registrations: Registration in SAM.gov is mandatory.  
- Required security clearances: Not specified.  
- Set-aside restrictions: Not specified.  
- Geographic restrictions: Not specified.  
- Minimum years of experience or past performance: Not specified.  
- Bonding or insurance requirements: Not specified.

**TECHNICAL CAPABILITIES:**  
Bidders should possess expertise in the production and handling of blood products, specifically Freeze Dried Plasma. Familiarity with FDA regulations and emergency use authorization processes is essential. Knowledge of relevant manufacturing standards and quality assurance protocols in the medical field is also critical.

**DELIVERABLES AND PERFORMANCE STANDARDS:**  
Key deliverables include the provision of Freeze Dried Plasma products that meet FDA standards for safety and efficacy. Specific milestones, reporting requirements, and performance metrics have not been detailed in the provided information.

**EVALUATION CRITERIA:**  
The evaluation criteria for proposals have not been explicitly outlined. However, bidders should prepare to demonstrate their technical approach, past performance, and pricing strategy, as these are typically key factors in government procurement evaluations.

**PREFERRED QUALIFICATIONS:**  
While not mandatory, bidders with experience in supplying medical products to military or government entities, as well as those with additional relevant certifications (e.g., ISO certifications related to quality management), may have a competitive advantage in the evaluation process.

In summary, potential bidders should ensure they are compliant with SAM.gov registration and possess the necessary technical capabilities in blood product manufacturing, while also preparing to demonstrate their qualifications and experience in similar projects.

Question 2

When is the proposal submission deadline?

Accepted Answer

The proposal submission deadline is March 25, 2026 (13 days left).

Question 3

What NAICS codes apply to this opportunity?

Accepted Answer

The applicable NAICS codes are: 325414.

Question 4

Are there any set-aside requirements?

Accepted Answer

Yes, this opportunity includes the following set-asides: NONE.

Question 5

Where can I submit a proposal or get solicitation documents?

Accepted Answer

You can access the full solicitation documents and submit your proposal at: https://sam.gov/workspace/contract/opp/ed19ca96864644109ee2c0d77f1ed018/view

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

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