Quality Assurance and Shelf-Life Compliance Testing
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The contract requires independent testing and documentation to validate the stability, concentration, and 12-month shelf-life compliance of a pharmaceutical product in accordance with Defense Logistics Agency standards. The work involves rigorous analytical procedures to ensure the product maintains its specified chemical integrity and efficacy over the designated shelf life, with all results formally documented to meet federal quality assurance requirements. Testing must be conducted by a qualified third party with demonstrated expertise in pharmaceutical stability protocols and regulatory compliance. This is a subcontract under the Medical Supply Chain Pharm FSA, part of the Department of Defense, solicited under NAICS code 541380 for other scientific and technical consulting services. The opportunity was posted on July 20, 2026, with responses due by July 27, 2026, and performance will be performed in support of national defense medical supply needs. All deliverables must align with DLA’s regulatory framework, and the contractor is expected to provide complete, auditable records to confirm adherence to shelf-life specifications without deviation.
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