| Location: | Maryland |
|---|---|
| Posted: | May 5, 2025 |
| Due: | May 19, 2025 |
| Agency: | HEALTH AND HUMAN SERVICES, DEPARTMENT OF |
| Type of Government: | Federal |
| Category: |
|
| Solicitation No: | NIHOD20250424WILLIAMETTI |
| Publication URL: | To access bid details, please log in. |
APEX Accelerators are an official government contracting resource for small businesses. Find your local APEX Accelerator (opens in new window) for free government expertise related to contract opportunities.
APEX Accelerators are funded in part through a cooperative agreement with the Department of Defense.
The APEX Accelerators program was formerly known as the Procurement Technical Assistance Program (opens in new window) (PTAP).
This is a Sources Sought Notice only. This notice is issued solely for market research and planning purposes under FAR Part 10 and does not constitute a solicitation. Responses to this notice will assist the government in determining the appropriate acquisition strategy, including whether a small business set-aside is appropriate.
Overview:
The National Institutes of Health (NIH) is conducting market research to identify qualified vendors capable of performing the contract requirement as stated in the attached statement of work.
A draft Statement of Work (SOW) is attached to provide additional details.
Please take a moment to thoroughly review the attached Statement of Work (SOW), which outlines the full scope and details of the drug formulation and manufacturing contract requirement.
Background:
The goal of the contract is to complete all the manufacturing, documentation, formulation, fill and finish, packaging, and labeling required for investigational drug products. Throughout the period of performance (PoP) of the contract, the contractor must maintain the technical capabilities, minimum resources and organizational compliances with which to successfully conduct any awarded contract activity. The contractor must also maintain a good standing as a “Qualified Vendor” as determined by ORSC. Additionally, unless otherwise requested, any assigned research must be performed in compliance with all current FDA, World Health Organization (WHO), USP, ISO, and International Committee on Harmonization (ICH) policies, practices, procedures, guidelines and regulations specific to current good manufacturing practices (cGMP) as may be applicable.
Clarifications:
As of now, there is no active contract in place for either the DFMC or the DMFP.
Submission Instructions
Interested parties should submit the following information no later than May 19, 2025 by 5:00pm Eastern Standard Time:
Disclaimer
This is not a request for proposal or quotation. This Sources Sought Notice does not commit the government to contract for any supply or service. The government will not reimburse any costs incurred in responding to this notice. Responses will not be returned. Not responding to this notice does not preclude participation in any future solicitation, if one is issued.
| Apr 24, 2025 | [Sources Sought (Original)] Drug Manufacturing and Formulation Contract II |
| Apr 28, 2025 | [Sources Sought (Updated)] Drug Formulation and Manufacturing Contract II (DFMC) |

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HEALTH AND HUMAN SERVICES, DEPARTMENT OF
Bid Due: 6/16/2026