Zdrowie i gospodarka · 15/09/2011

FDA Releases Draft Guidance on Electronic Data Transfer for Veterinary Medicinal Products

The US Food and Drug Administration (FDA) has made available a draft guidance document, VICH GL35, which outlines electronic standards for transferring data related to adverse event reports for veterinary medicinal products, developed by the International Cooperation on Harmonisation of Technical Requirements for Registration of Veterinary Medicinal Products (VICH).