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This Government Contract opportunity from Department Of Veterans Affairs was posted on June 3, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Regulatory Compliance & Certification Services

Closed
Federal

Contract Overview

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This contract involves providing comprehensive regulatory compliance and certification services focused on medical devices. The scope includes testing, verification, and documentation to ensure adherence to multiple important standards including FDA, IEC, UL/ETL, FCC, and CE Mark requirements. The objective is to guarantee that medical devices meet all necessary regulatory criteria before market release or continued distribution. The subcontract is overseen by the Department of Veterans Affairs through their 261-NETWORK Contract Office 21. It was posted on June 3, 2026, with a response deadline set for June 8, 2026. The place of performance is specified as Concord, with the NAICS code 541380 indicating the contract relates to engineering services. This opportunity is geared toward entities capable of providing specialized testing and certification consulting within the medical device regulatory framework.

General Info

Provide medical device regulatory compliance, testing, and certification services per FDA, IEC, UL, FCC, CE.

Agency

Department Of Veterans Affairs → 261-NETWORK Contract Office 21 (36C261)

NAICS

541380 - Testing Laboratories and ServicesView NAICS

Place of Performance

Concord, CA, 95928, 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 Veterans Affairs → 261-NETWORK Contract Office 21 (36C261)
ContactsNo contacts available
OfficeN/A
Organization / Agency
Department Of Veterans Affairs → 261-NETWORK Contract Office 21 (36C261)
Office AddressN/A
ContactsNo contact information available

Full Description

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Provide testing, verification, and documentation of compliance with FDA, IEC, UL/ETL, FCC, and CE Mark standards for medical devices.