Zdrowie i gospodarka · 23/05/2024

FDA Announces Draft Guidance for Industry on Reproduction Testing of Veterinary Drug Residues in Human Food

The US Food and Drug Administration (FDA) has released a draft revised guidance (GFI #115) for the evaluation of the safety of residues of veterinary drugs in human food, focusing on reproduction testing, developed by the International Cooperation on Harmonisation of Technical Requirements for Registration of Veterinary Medicinal Products (VICH).

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

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