Veterinary medicines
date: 02/10/2024
Marketing authorisation holders are required to manually add the email addresses of the Qualified Person for Pharmacovigilance (QPPV) for their products to the Union Product Database by 31 October 2024. This information will be used to send advice notes, listings of chargeable units line, and other supporting communications resulting from the forthcoming Regulation (EU) 2024/568 on fees and charges payable to the European Medicines Agency.
The EU Implementation Guide on veterinary product data in the UPD has been updated accordingly. To request assistance marketing authorisation holders are advised to contact the relevant national competent authority (a list of Member States’ UPD contact points is available here). To contact the EMA, please use the EMA Service Desk (ServiceNow).