PK IDIQ- Post-market Bioequivalence of Generic Drug Products
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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 multiple-award Indefinite-Delivery, Indefinite-Quantity (IDIQ) contract for post-market bioequivalence studies of generic drug products. This contract will support the agency’s mission to ensure the safety, efficacy, and therapeutic equivalence of generic drugs after they enter the market. The effort is classified under NAICS code 541714, indicating it involves research and development in the physical, engineering, and life sciences. The work will primarily involve pharmacokinetic studies to assess how generic drugs behave in the human body compared to their brand-name counterparts, with performance expected to occur across various locations without a designated primary city or state. The solicitation is not yet open, with a posted date of May 25, 2026, indicating this is a pre-solicitation forecast. There is no set-aside designation specified, meaning the contract is open to all eligible businesses. The point of contact for program-related inquiries is the Cder Acquisition Liaison, reachable at cderacquisitions@fda.hhs.gov, while the contracting officer’s details remain to be determined. Interested parties should monitor the official OSDBU portal for the upcoming solicitation, as this forecast serves as an early notice to industry stakeholders to prepare proposals and align resources for future contract awards under this IDIQ vehicle.
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