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This Government Contract opportunity from Department Of Veterans Affairs was posted on May 13, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Regulatory Compliance & Quality Assurance Support

Closed
Federal

Contract Overview

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This contract involves providing ongoing regulatory and quality assurance support to ensure compliance with medical device standards, specifically related to FDA 21 CFR Part 820. The work includes critical activities such as adverse event reporting, conducting audits, and managing post-market surveillance for medical devices supplied to the Department of Veterans Affairs. The services aim to maintain high standards of safety and efficacy for devices used within the VA system. The contract is categorized under NAICS code 541690 and is structured as a subcontract. It is managed by the 260-NETWORK Contract Office 20 within the Department of Veterans Affairs, with the place of performance located in Portland, zip code 97239. The solicitation was posted on May 13, 2026, with a response deadline of May 26, 2026, at 3:00 PM. This contract ensures continuous support to meet regulatory requirements and uphold quality assurance protocols in the VA’s medical device supply chain.

General Info

Provide regulatory and quality assurance support for VA medical devices under FDA 21 CFR Part 820 compliance.

Agency

Department Of Veterans Affairs → 260-NETWORK Contract Office 20 (36C260)

NAICS

541690 - Other Scientific and Technical Consulting ServicesView NAICS

Place of Performance

Portland, WA, 97239

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 Veterans Affairs → 260-NETWORK Contract Office 20 (36C260)
ContactsNo contacts available
OfficeN/A
Organization / Agency
Department Of Veterans Affairs → 260-NETWORK Contract Office 20 (36C260)
Office AddressN/A
ContactsNo contact information available

Full Description

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Ongoing regulatory and quality support for medical device compliance, including FDA 21 CFR Part 820, adverse event reporting, audits, and post-market surveillance for devices supplied to the VA.