Labeling Pilot for FDF Country of Origin, API Country of Origin, and KSM Country of Origin for Pharmaceutical Products

Closed Pre-Solicitation Posted

Solicitation number
DLATS-RFI-MSC
Agency
Responses due
Set-aside
No set-aside

Opportunity facts

NAICS code
Not on record
PSC
Not on record
Place of performance
Philadelphia, Pennsylvania, United States

Notice details come from SAM.gov. Updated .

About this opportunity

The Defense Logistics Agency Troop Support Medical Supply Chain is conducting market research through a Request for Information due September 23, 2026 to identify U.S. or international pharmaceutical manufacturers willing to participate in a labeling pilot program exploring voluntary inclusion of country-of-origin data for pharmaceutical products.

The pilot focuses on a selected subset of generic pharmaceutical products and requests manufacturers provide country of origin for the Finished Dose Form, country of origin for each Active Pharmaceutical Ingredient, and country of origin for each Key Starting Material necessary for API production. DLA will accept alternative methods of providing this information, including QR codes or links to supplemental documentation. When API or KSM country of origin varies by lot, manufacturers should supply lot-specific information for both labeled and previously produced lots.

DLA Troop Support Medical is evaluating labeling enhancements to improve supply chain transparency, enhance traceability, and strengthen operational readiness through increased visibility into pharmaceutical ingredient sourcing. The agency identifies this capability as supporting contingency planning, risk modeling, and alignment with emerging regulatory and strategic sourcing initiatives.

This RFI is issued solely for information and planning purposes and does not constitute a solicitation or commit the Government to any future acquisition or requirement. No set-aside is anticipated.

Notice text

1. Purpose

The Defense Logistics Agency (DLA) Troop Support Medical Supply Chain is conducting market research to identify U.S. or international pharmaceutical manufacturers that are willing to participate in a labeling pilot program. The pilot seeks to explore voluntary inclusion of additional product labeling data for Pharmaceutical Products identifying:

  • Country of origin for the Finished Dose Form (FDF)
  • Country of origin for each Active Pharmaceutical Ingredient (API)
  • Country of origin for each Key starting material (KSM) necessary for the production of each API
  • Given the amount of information requested, inclusion of a QR code or link to additional information, or other methods of making the information accessible, could be considered
  • If the country of origin of the API or KSM can vary by lot produced, DLA would be interested in the information specific to the labeled lot and to any previously produced lots

This RFI is issued solely for information and planning purposes. It does not constitute a solicitation, and responses do not commit the Government to any future acquisition or requirement.

2. Background

DLA Troop Support Medical is evaluating methods to improve supply chain transparency, enhance traceability, and strengthen operational readiness by increasing visibility into the sourcing of pharmaceutical ingredients. Understanding FDF, API, and KSM origins helps support contingency planning, risk modeling, and alignment with emerging regulatory and strategic sourcing initiatives.

The agency is exploring the feasibility of obtaining this information directly from manufacturers through voluntary labeling enhancements on packaging, shipping containers, or supplemental documentation.

3. Scope of Pilot

The proposed labeling pilot will focus on a selected subset of generic pharmaceutical products purchased by DLA Troop Support Medical. Participating manufacturers may be asked to provide:

  • API country of manufacture
  • API country of origin (if different)
  • Country of origin for the Finished Dose Form (FDF)
  • Country of origin for each Key starting material (KSM) necessary for the production of each API
  • If the country of origin of the API or KSM can vary by lot produced, DLA would be interested in the information specific to the labeled lot and to any previously produced lots
  • Placement of this information on external packaging, product containers, or accompanying supply chain documentation
    • Given the amount of information requested, inclusion of a QR code or link to additional information, or other methods of making the information accessible, could be considered
  • Estimated production or administrative impact associated with adding these data elements

DLA seeks to understand both operational feasibility and industry readiness.

4. Requested Information from Respondents

Interested manufacturers are invited to submit a written response addressing the following:

A. Company name, CAGE code, point of contact information
B. Description of the pharmaceutical products you manufacture that are supplied or could be supplied to DLA
C. Willingness to participate in a voluntary labeling or data‑sharing pilot to include:

  • Development of a labeling construct that contains all relevant sourcing information as outlined below.
  • Obtaining approval of the labeling construct from the Food and Drug Administration.
  • Producing labels with all required sourcing information and affixing them to products sold to the Department of War.

D. Ability to provide the following information for each lot produced:

  • API country of manufacture
  • API country of origin (if different)
  • Country of origin for the Finished Dose Form (FDF)
  • Country of origin for each Key starting material (KSM) necessary for the production of each API
  • If the country of origin of the API or KSM can vary by lot produced, DLA would be interested in the information specific to the labeled lot and to any previously produced lots
  • Placement of this information on external packaging, product containers, or accompanying supply chain documentation
    • Given the amount of information requested, inclusion of a QR code or link to additional information, or other methods of making the information accessible, could be considered
  • Estimated production or administrative impact associated with adding these data elements
  • E. Existing internal capabilities or systems that support API and KSM traceability and documentation
    F. Expected timeline and level of effort required to implement labeling modifications
    G. Any concerns, limitations, or cost impacts associated with participation
    H. Recommendations for structuring or scaling the pilot program

5. Submission Instructions

Responses should be submitted via email in PDF or Word format to the DLA Troop Support Medical Supply Chain point of contact:

Contracting Officer:
Charles T. Reimer
DLA Troop Support – Medical Supply Chain
Email: Charles.Reimer@dla.mil
Phone: 267-251-9370 (Cell)

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