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BPA - HPLC/UHPLC and GC-MS Systems

Forecast

Federal

Contract Overview

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This Blanket Purchase Agreement for the Food and Drug Administration involves the acquisition of new HPLC/UHPLC and GC-MS systems to support OLOAS operations. The contract structure consists of a base period with four option years. These advanced instruments are intended to increase sample throughput, enhance laboratory efficiency for complex chemical analyses, and improve the overall sample flow process for regulatory samples to enable faster decision-making. The procurement aims to strengthen the quality and defensibility of analytical results through improved sensitivity, selectivity, and reliability of the instrumentation. This effort falls under NAICS code 334516 and is managed by the FDA, with the primary goal of reducing turnaround times for multi-residue screening and targeted quantitative methods to better support regulatory actions.

General Info

FDA blanket purchase agreement for HPLC/UHPLC and GC-MS systems to improve laboratory efficiency.

Agency

Food and Drug Administration → Food And Drug Administration

NAICS

334516 - Analytical Laboratory Instrument Manufacturing

Place of Performance

USA

Set-Aside

NONE

Documents

0

No documents available

Documents will appear here when they are available.

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Organization & Contact Information

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AgencyFood and Drug Administration → Food And Drug Administration

Contacts2 people available

OfficeN/A

Organization / AgencyFood and Drug Administration → Food And Drug Administration

Office AddressN/A

Contacts

Hfp Acquisition Liaison

contact@example.gov

To Be Determined To Be DeterminedContracting Officer

Full Description

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BPA - HPLC/UHPLC and GC-MS Systems Base + 4 OY The acquisition of new HPL>C/UHPLC and GC-MS systems will provide several benefits to OLOAS operations. First these advanced instruments will increase sample throughput by enabling faster analysis times and the capability to process multiple samples simultaneously. Second, the new system will enhance OLOAS laboratory's efficiency and speed in conducting complex chemical analyses, including multi-residue screening and targeted quantitative methods. Third, the improved instrumentation will lead to an overall enhanced sample flow process for regulatory samples, reducing turnaround times and enabli8ng more rapid regulatory decision-making. Additionally, modern HPLC/UHPLC and GC-MS systems offer improved sensitivity, selectivity, and reliability, which will strengthen the quality and defensibility of analytical results supporting FDA's regulatory actions.

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