Rolnictwo i żywność · 22/10/2010

Draft Guidelines on Pharmacovigilance of Veterinary Medicinal Products: Electronic Standards for Transfer of Data

The International Cooperation on Harmonization of Technical Requirements for the Registration of Veterinary Medicinal Products (VICH) has released a draft guideline for the electronic transfer of adverse event reports on veterinary biologics between regulatory authorities in the European Union, Japan, and the United States and marketing authorization holders. The US Department of Agriculture's Animal and Plant Health Inspection Service is seeking public comments on the draft guideline.