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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 Compliance Support (Medical Devices)

Closed
Federal

Contract Overview

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This contract involves providing consulting services focused on ensuring compliance with key regulatory and technical standards applicable to medical device contracts, including DFARS, NIST SP 800-171, FDA Quality System Regulation, and Defense Logistics Agency requirements. The support aims to assist the medical supply chain under the Department of Defense in meeting these stringent guidelines to maintain quality, security, and regulatory adherence. The work will be conducted as a subcontract under NAICS code 541611, with the place of performance located in Annville, identified by the 17003-5003 ZIP code. The contract is managed by the Medical Supply Chain MD Surg FSF office within the Department of Defense. Interested parties must respond by June 8, 2026, shortly after the solicitation was posted on May 31, 2026. Additional details and submission instructions are available through the provided DLA Business Systems link.

General Info

Consulting services to ensure DoD medical device compliance with DFARS, NIST, FDA, and DLA standards.

Agency

Department Of Defense → MEDICAL SUPPLY CHAIN MD SURG FSF

NAICS

541611 - Administrative Management and General Management Consulting Services View NAICS

Place of Performance

ANNVILLE, PA, 17003-5003, 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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Consulting services to ensure compliance with DFARS, NIST SP 800-171, FDA QSR, and DLA technical requirements for medical device contracts.