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This Government Contract opportunity from Department Of Defense was posted on May 20, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Regulatory and Quality Compliance Management

Closed
Federal

Contract Overview

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The contract entails ongoing management of regulatory compliance for supplied medical devices, focusing on critical areas such as Unique Device Identification (UDI) labeling, adverse event reporting, lot traceability, and ensuring audit readiness. This comprehensive approach aims to maintain adherence to regulatory standards and streamline quality management processes for medical devices used by the Defense Health Agency under the Department of Defense. The subcontract, categorized under NAICS code 541611, is set to be performed in Portsmouth, with a response deadline scheduled for May 25, 2026. It involves continuous oversight of compliance-related activities to support the Defense Health Agency's mission and operational requirements. The contract underscores the importance of maintaining robust quality systems in the healthcare supply chain to enhance patient safety and regulatory accountability.

General Info

Ongoing regulatory compliance management for Defense Health Agency medical devices, focusing on UDI, reporting, traceability.

Agency

Department Of Defense → Defense Health Agency

NAICS

541611 - Administrative Management and General Management Consulting Services View NAICS

Place of Performance

Portsmouth, VA, 23708, USA

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 → Defense Health Agency
ContactsNo contacts available
OfficeN/A
Organization / Agency
Department Of Defense → Defense Health Agency
Office AddressN/A
ContactsNo contact information available

Full Description

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Ongoing management of regulatory compliance for supplied medical devices, including UDI labeling, adverse event reporting, lot traceability, and audit readiness.