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This Government Contract opportunity from Department Of Veterans Affairs was posted on May 1, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Quality Assurance and Regulatory Compliance Support

Closed
Federal

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This contract involves providing independent validation services for sequencing results, ensuring the accuracy and integrity of the data through thorough audit trail documentation. It further supports compliance with established research standards such as Good Laboratory Practice (GLP) and Clinical Laboratory Improvement Amendments (CLIA). The contract is a subcontract issued by the Department of Veterans Affairs under the NAICS code 541611, focusing on management and technical consulting services. The work will be performed in Portland, with a response deadline set for mid-May 2026. The contract aims to reinforce quality assurance and regulatory compliance within research operations, particularly by validating sequencing outputs and maintaining detailed records that adhere to federal research standards. This will help ensure the credibility and regulatory adherence of laboratory results critical to the department’s research initiatives.

General Info

Provide independent sequencing validation and audit to ensure GLP, CLIA compliance for VA subcontract.

Agency

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

NAICS

541611 - Administrative Management and General Management Consulting Services View 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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Independent validation of sequencing results, audit trail documentation, and support for compliance with research standards such as GLP or CLIA.