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Regulatory Compliance & Certification Support

Active

Federal

Response Deadline08/21/2026, 03:00:00 PM UTC

Contract Overview

Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.

AI Contract Overview

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The Department of Veterans Affairs, through the NETWORK Contract Office 4, is seeking a subcontractor to provide professional consulting support for regulatory compliance and certification. The primary objective of this engagement is to ensure that medical devices achieve and document compliance with ISO 60601-1, CSA/CE Class 1, and other relevant medical device regulatory standards. This opportunity is categorized under NAICS code 541690 and will be performed in Pittsburgh, Pennsylvania. Interested parties must submit their responses by the deadline of August 21, 2026, at 3:00 PM.

General Info

VA seeks subcontractor for medical device regulatory compliance and certification in Pittsburgh, PA.

Agency

Department Of Veterans Affairs → 244-NETWORK Contract Office 4 (36C244)View Agency

NAICS

541690 - Other Scientific and Technical Consulting ServicesView NAICS

Place of Performance

Pittsburgh, PA, 15206

Set-Aside

NONE

Documents

This scope was carved out of 36C24426Q0849.

The full solicitation package (1 document), including the RFP, is on the prime solicitation, not on this scope.

View the prime solicitation

AN12--Flexible wheelchair cushion pressure sensor mat

AI Contract Breakdown

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Timeline

PostedAug 17

subcontract

Response DeadlineAug 21

Submission deadline

Response Deadline

08/21/2026, 03:00:00 PM UTCin 4 days

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Organization & Contact Information

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AgencyDepartment Of Veterans Affairs → 244-NETWORK Contract Office 4 (36C244)

ContactsNo contacts available

OfficeN/A

Organization / Agency

Department Of Veterans Affairs → 244-NETWORK Contract Office 4 (36C244)

View Agency Profile

Office AddressN/A

ContactsNo contact information available

Full Description

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Consulting support for achieving and documenting compliance with ISO 60601-1, CSA/CE Class 1, and related medical device regulatory standards.

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