Zdrowie i gospodarka · 12/04/2010

FDA Releases Draft Guidance for Evaluating Veterinary Drug Metabolism in Laboratory Animals

The FDA has made available a draft guidance document, VICH GL47, developed by the International Cooperation on Harmonisation of Technical Requirements for Registration of Veterinary Medicinal Products, to provide internationally harmonized procedures for identifying veterinary drug metabolites in laboratory animals for comparison to food animal residues.