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This Government Contract opportunity from Department Of Defense was posted on May 27, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Regulatory Compliance and Quality Assurance for Medical Supplies

Closed
Federal

Contract Overview

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This contract involves ensuring that medical items comply with key regulatory requirements set by the FDA, DLA, and DFARS, focusing on labeling, packaging, documentation, and quality assurance specifically for regulated medical devices. The work is associated with regulatory compliance and quality assurance for medical supplies, aligning with NAICS code 541611, which pertains to management and consulting services. The subcontract is posted by the Department of Defense under the Medical Supply Chain MD SURG FSF division and the place of performance is Fort Bragg, zip code 28310. The solicitation was posted on May 27, 2026, with a response deadline of June 2, 2026. This contract emphasizes adherence to federal standards to ensure medical devices meet required quality and regulatory benchmarks, supporting military medical supply chains.

General Info

Ensure FDA, DLA, DFARS compliance for medical device labeling, packaging, documentation, quality at Fort Bragg.

Agency

Department Of Defense → MEDICAL SUPPLY CHAIN MD SURG FSF

NAICS

541611 - Administrative Management and General Management Consulting Services View 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 MD SURG FSF
ContactsNo contacts available
OfficeN/A
Organization / Agency
Department Of Defense → MEDICAL SUPPLY CHAIN MD SURG FSF
Office AddressN/A
ContactsNo contact information available

Full Description

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Ensure medical items meet FDA, DLA, and DFARS requirements including labeling, packaging, documentation, and quality assurance for regulated medical devices.