Regulation & law · 01/12/2000

Draft Guideline on Pharmacovigilance of Veterinary Medicinal Products: Management of Adverse Event Reports

The International Cooperation on Harmonization of Technical Requirements for Registration of Veterinary Medicinal Products (VICH) has developed a draft guideline on managing adverse event reports for veterinary medicinal products. The US Department of Agriculture is seeking public input on the draft to inform its comments to the VICH Steering Committee.