Pharmacovigilance-related recommendations to product information for centrally authorised veterinary medicines
The European Medicines Agency's (EMA) Committee for Veterinary Medicinal Products (CVMP) issues recommendations on updating the product information for centrally authorised veterinary medicines, based on an evaluation of safety data. The marketing authorisation holder of the medicine is responsible for implementing these CVMP recommendations.
Legal Disclaimer:
EIN Presswire provides this news content "as is" without warranty of any kind. We do not accept any responsibility or liability for the accuracy, content, images, videos, licenses, completeness, legality, or reliability of the information contained in this article. If you have any complaints or copyright issues related to this article, kindly contact the author above.
