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DBPAP // UltiMate 3000 HPLC (MA)

Active

Federal

Contract Overview

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

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The Food and Drug Administration is forecasting a requirement for specific mass spectrometers and HPLC systems, including the Synapt G2, MALDI ToF, LTQ XL, GC, HPLC 3000RS, and HPLC 1200. These instruments are essential for mission critical research focused on vaccine antigens and host-pathogen interactions. The primary objectives of the studies include analyzing antigen structure and the influence of post translational modifications on viral pathogen receptor interactions, host ligand preferences, and the pathogen's interaction with host innate immune system collections. This procurement is categorized under NAICS code 811219 and is managed by the CBER Acquisition Liaison.

General Info

FDA seeks mass spectrometers and HPLC systems for vaccine and pathogen research.

Agency

Food and Drug Administration → Food And Drug Administration

NAICS

811219 - Other Electronic and Precision Equipment Repair and Maintenance

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

Cber Acquisition Liaison

contact@example.gov

To Be Determined To Be DeterminedContracting Officer

Full Description

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The listed mass spectrometers (Synapt G2, MALDI ToF, LTQ XL, GC) and HPLC (HPLC 3000RS and HPCL 1200) systems are required for mission critical studies to investigate three areas involving vaccine antigens and host-pathogen interactions. These are the study of: 1) antigen structure and how it is effected by post translational modifications; 2) post translational modifications effect on viral pathogen receptor interaction and host ligand preferences and; 3) post translational modification impact on pathogen interaction with host innate immune system collections. Center Unfunded Requirement

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