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Quality Control and Analytical Testing Services

Active
Federal

Contract Overview

Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.

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This contract involves subcontracted quality control and analytical testing services specifically for the pharmaceutical industry. It mandates third-party testing of drug batches to ensure potency, purity, sterility, and stability prior to release, in full compliance with current Good Manufacturing Practice (cGMP) standards. The testing is critical for safeguarding that drug products meet regulatory requirements and maintain their efficacy and safety before reaching the market. Issued by the Department of Veterans Affairs under the Nac Federal Supply Schedule (36F797), the contract falls under NAICS code 541380, which pertains to testing laboratories. Although specific location details and points of contact are not provided, the subcontract arrangement emphasizes adherence to stringent federal quality standards. This service plays a key role in the pharmaceutical supply chain by providing reliable verification of drug quality for subsequent distribution and use.

General Info

Subcontract for pharmaceutical quality control testing ensuring drug compliance with cGMP standards.

NAICS

541380 - Testing Laboratories and Services

Place of Performance

IL

Set-Aside

NONE

Documents

This scope was carved out of 36F79726D0137.

The full solicitation package (1 document), including the RFP, is on the prime solicitation, not on this scope.

View the prime solicitation

6505--Ipsen Biopharmaceuticals, Inc., dba Tercica, Inc. 65IB 36F79726D0137 Effective: 06/01/2026-05/31/2031

AI Contract Breakdown

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Timeline

Posted

subcontract

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Organization & Contact Information

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AgencyDepartment Of Veterans Affairs → Nac Federal Supply Schedule (36F797)
ContactsNo contacts available
OfficeN/A
Office AddressN/A
ContactsNo contact information available

Full Description

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Third-party testing for potency, purity, sterility, and stability of drug batches prior to release under cGMP requirements.

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