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Fisher BPA

Active
Federal

Contract Overview

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The Food and Drug Administration has established a one-year general laboratory consumables purchase agreement with Fisher Scientific to support OPQR testing of medicines approved for human use. This contract provides essential reagents and consumables for STL, WO, and AMRF testing capabilities, ensuring that analytical laboratories have the necessary supplies for regular surveillance of the US drug supply, compliance actions, and rapid response requirements. By utilizing a vendor widely used by laboratory staff, the agreement streamlines the procurement process and eliminates the need for PCARD transactions, thereby increasing overall testing throughput. This initiative directly supports the operational needs of the PDUFA and GDUFA user fee programs to maintain the quality and safety of human medicines.

General Info

FDA one-year agreement with Fisher Scientific for laboratory consumables to support medicine testing.

NAICS

325199 - All Other Basic Organic Chemical Manufacturing

Place of Performance

USA

Set-Aside

NONE

Documents

0

No documents 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
Office AddressN/A
Contacts
Cder Acquisition Liaison
To Be Determined To Be DeterminedContracting Officer

Full Description

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A general laboratory consumables purchase agreement for OPQR testing to support agency mission relevant testing of the quality of medicines approved for human use. The contract will support STL, WO and AMRF testing capabilities by suppling common laboratory reagents and consumables used by analytical testing laboratories. Use of purchasing aggreement with a vendor that is widely used by lab staff (Fisher Scientific) for the period of the 1 year contract enhances efficiency by simplifying the lab supply purchasing process (no PCARD needed). The agreement would also enhances testing throughput by assuring critical reagents and consumables are on hand as needed for rapid response actions, testing for compliance actions and testing that is part of the regular surveillance of the US drug supply. The contract supports PDUFA and GDUFA user fee program needs.

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