DBPAP // UltiMate 3000 HPLC (MA) / Jankowska - New Requirement
Past New Requirement Updated
- Agency
-
Food and Drug Administration
Department of Health and Human Services
- Solicitation expected
- Estimated value
- $10,000 to $25,000
- Set-aside
- No set-aside
Forecast facts
- Anticipated award
- NAICS code
- 334516 Analytical Laboratory Instrument Manufacturing
- Points of contact
-
- Joshua Holliday joshua.holliday@fda.hhs.gov
Forecast details come from HHS's procurement forecast. Agencies' dates and values are estimates.
About this forecast
The Food and Drug Administration is seeking to procure mass spectrometers and HPLC systems for critical scientific research focused on vaccine antigen studies and host-pathogen interactions. The procurement targets specific analytical laboratory instruments including Synapt G2, MALDI ToF, LTQ XL, GC, HPLC 3000RS, and HPCL 1200 systems to investigate three key research areas involving antigen structure, post-translational modifications, and pathogen-host immune system interactions. The estimated solicitation release date is July 1, 2026, with an anticipated contract award date of September 1, 2026.
This is currently an unfunded center requirement within the Department of Health and Human Services, categorized under NAICS code 334516 for Analytical Laboratory Instrument Manufacturing. The point of contact for this potential opportunity is Joshua Holliday, who can be reached at joshua.holliday@fda.hhs.gov within the FDA organization. While specific award values or precise quantities are not currently disclosed, the procurement appears to be mission-critical for advanced scientific research purposes, suggesting potential significant investment in sophisticated laboratory instrumentation.
Forecast text
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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