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Zdrowie i gospodarka · 27/03/2024

FDA Releases Guidance on Handling and Retention of Bioavailability and Bioequivalence Testing Samples

The FDA has published a guidance document outlining procedures for handling and retaining reserve samples from bioavailability and bioequivalence studies for new drug applications, abbreviated new drug applications, and contract research organizations.

Source: Federal Register — Food and Drug AdministrationOpen original release →