Zdrowie i gospodarka · 05/03/2013

FDA Announces Draft Revised Guidance on Genotoxicity Testing for Veterinary Drugs in Human Food

The Food and Drug Administration (FDA) has released a draft revised guidance for industry (GFI 116) on evaluating the safety of residues of veterinary drugs in human food, specifically focusing on genotoxicity testing. This revised guidance updates a previous final guidance published in 2002 and is developed by the International Cooperation on Harmonisation of Technical Requirements for Registration of Veterinary Medicinal Products (VICH).