Zdrowie i gospodarka · 01/06/2015

FDA Announces Draft Guidance for Evaluating Residues of Veterinary Drugs in Human Food

The Food and Drug Administration (FDA) has released a draft guidance document, VICH GL54, to help establish an acute reference dose (ARfD) for residues of veterinary drugs in human food, developed by the International Cooperation on Harmonisation of Technical Requirements for Registration of Veterinary Medicinal Products (VICH)