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This Government Contract opportunity from Department Of Defense was posted on May 31, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Regulatory and Quality Assurance Support

Closed
Federal

Contract Overview

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This subcontract opportunity titled "Regulatory and Quality Assurance Support" issued by the Department of Defense's Medical Supply Chain Pharm FSA focuses on providing essential pre-award and ongoing regulatory documentation. The scope includes the submission of Material Safety Data Sheets (MSDS) or Safety Data Sheets (SDS), packaging test reports, and compliance certifications in alignment with Defense Logistics Agency (DLA) requirements. The contract is categorized under NAICS code 541690, indicating specialized consulting services related to regulatory compliance and quality assurance. The solicitation was posted on May 31, 2026, with a response deadline set for June 8, 2026. The work is to be performed in Fort Bragg, ZIP code 28310. This subcontract does not specify any set-aside type or organizational type preferences. It aims to support regulatory assurance functions critical to the medical supply chain, ensuring products meet all necessary safety and compliance standards throughout the award lifecycle.

General Info

Provide regulatory documentation and quality assurance for medical supply chain at Fort Bragg.

Agency

Department Of Defense → MEDICAL SUPPLY CHAIN PHARM FSA

NAICS

541690 - Other Scientific and Technical Consulting ServicesView NAICS

Place of Performance

FORT BRAGG, NC, 28310, US

Set-Aside

NONE

Documents

(0)

No documents available

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Timeline

PhaseClosed
Posted

subcontract

Response Deadline

Deadline has passed

Submission Closed

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Organization & Contact Information

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AgencyDepartment Of Defense → MEDICAL SUPPLY CHAIN PHARM FSA
ContactsNo contacts available
OfficeN/A
Organization / Agency
Department Of Defense → MEDICAL SUPPLY CHAIN PHARM FSA
Office AddressN/A
ContactsNo contact information available

Full Description

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Provide pre-award and ongoing regulatory documentation, including submission of MSDS/SDS, packaging test reports, and compliance certifications per DLA requirements.