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This Government Contract opportunity from Department Of Health And Human Services was posted on August 5, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Operational Qualification / Performance Verification (OQ/PV) Services

Closed
Federal

Contract Overview

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This contract outlines the provision of Operational Qualification and Performance Verification (OQ/PV) services for Agilent Gas Chromatography (GC) systems following maintenance or repair activities. The objective is to verify that the instruments meet the manufacturer's technical specifications and comply with stringent regulatory standards required by FDA-regulated laboratories. The scope includes the execution of standardized testing protocols, accurate collection and documentation of performance data, and the generation of comprehensive final reports that demonstrate system compliance and readiness for use in regulated environments. All testing must be conducted with rigor to ensure data integrity, instrument accuracy, and alignment with federal laboratory requirements. The contract is issued under NAICS code 541380, categorizing it as a scientific and technical consulting service, and is structured as a subcontract within the Department of Health and Human Services framework administered by the FDA Office of Acquisition and Grant Services. The place of performance is specified as 30310, indicating the work is tied to a specific facility or region, though exact location details are not provided. The solicitation was posted August 5, 2026, with responses due by August 19, 2026, setting a clear timeline for interested parties to submit proposals. While no set-aside status or point of contact details are listed, the contractual requirement emphasizes regulatory adherence, precise documentation, and technical expertise to support the continued reliability of analytical instrumentation in critical testing environments.

General Info

OQ/PV services for Agilent GC systems to ensure FDA-compliant performance after maintenance.

NAICS

541380 - Testing Laboratories and Services

Place of Performance

GA, 30310, USA

Set-Aside

NONE

Documents

This scope was carved out of OC-2026-134506.

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

View the prime solicitation

Preventive Maintenance of existing Agilent Equipment (Brand Name or Equal Service)

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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 Health And Human Services → FDA Office Of Acq Grant Svcs
ContactsNo contacts available
OfficeN/A
Office AddressN/A
ContactsNo contact information available

Full Description

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Formal OQ/PV testing for Agilent GC systems post-maintenance or repair to ensure compliance with manufacturer and FDA laboratory standards, including test execution, data collection, and report generation.

More opportunities from Department Of Health And Human Services → FDA Office Of Acq Grant Svcs

Same awarding agency

NAICS: 541611
New
Federal
Contractor-Hosted Fully Integrated Records Facility (FIRF) IDIQ
Solicitation # 75F40126R00009
Solicitation 75F40126R00009 is a request for proposals for a single Indefinite Delivery, Indefinite Quantity (IDIQ) contract to provide Contractor-Hosted Fully Integrated Records Facility (FIRF) services for the FDA. This acquisition is exclusively set aside for Service-Disabled Veteran-Owned Small Business (SDVOSB) concerns under NAICS code 541611. The contract has a maximum ceiling of 50 million dollars with a guaranteed minimum of 10,000 dollars. The anticipated period of performance consists of five 12-month ordering periods from December 1, 2026, through November 30, 2031, with an additional six-month option to extend services through May 31, 2032. The contract will support various task order types, including Time-and-Materials, Labor-Hour, and Firm-Fixed Price. The scope of work requires the contractor to manage an offsite document control facility to standardize records management and transition the agency toward a near 100 percent electronic environment for premarket and postmarket submissions. Key task areas include program management, document processing, scanning, data entry, tracking, temporary storage, and transition activities. Performance will primarily occur at FDA facilities in the Washington, D.C. metropolitan area, specifically within Maryland. Award will be made on a Lowest Price-Technically Acceptable (LPTA) basis, evaluating technical factors and past performance on an acceptable or unacceptable basis. Proposals must be submitted electronically in three separate volumes, with a final submission deadline of November 5, 2026, at 2:00 PM Eastern Time.
Administrative Management and General Management Consulting Services

POSTED

1 day ago

DEADLINE

in 8 days
View Details

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