Opportunity
SAM #HPF-2026-135452
FDA Solicits Custom ISO 17034 Analytical Reference Standards for Veterinary Drug Residue Analysis
Buyer
FDA Office of the Associate General Counsel for Administrative Law
Posted
August 04, 2026
Respond By
August 07, 2026
Identifier
HPF-2026-135452
NAICS
325412, 325413, 325998
The FDA Denver Human and Animal Food Laboratory (DENHAFL), part of the Department of Health and Human Services, is seeking vendors to supply custom-prepared, multi-component analytical reference standard solutions for regulatory analysis of veterinary drug residues in aquaculture, dairy, and game-meat products. - Government Buyer: - Food and Drug Administration (FDA), Human and Animal Food (HFP) network, Denver Human and Animal Food Laboratory (DENHAFL) - Products/Services Requested: - Custom-prepared, multi-component analytical reference standard solutions for veterinary drug residue analysis - 15 distinct multi-component standard mixtures, each delivered as two lots (Initial Calibration Verification [ICV] and Continuing Calibration Verification [CCV]) - Each lot contains five 1 mL glass ampules, totaling approximately 150 ampules - Drug classes include: NSAIDs, Macrolides, Amphenicols, Avermectins, Nitroimidazoles, Quinolones, Fluoroquinolones, Sulfonamides - All standards must be ISO 17034 accredited, dissolved in LC-MS-grade solvents, and sealed in 1 mL glass ampules - Unique/Notable Requirements: - All standards must have a minimum 12-month shelf life; those with less must be replaced at no additional cost before expiration - Delivery required to DENHAFL on or about the specified date - Solutions are for use in both screening and confirmatory LC-MS methods for regulatory analysis - No specific OEMs or vendors are named in the solicitation - All technical and compliance requirements are detailed in the attached documents
Description
The Food and Drug Administration (FDA) Denver Human and Animal Food Laboratory (DENHAFL) requires custom-prepared, multi-component analytical reference standard solutions for use in the regulatory analysis of veterinary drug residues in aquaculture, dairy, and game-meat products. The standards support initial calibration verification (ICV) and continuing calibration verification (CCV) in screening and confirmatory liquid chromatography–mass spectrometry (LC-MS) methods.