Release notes - production release version 1.7.2514-3 - 21 March 2025 - Veterinary Medical Products Regulation: Union Product Database
Mandate, objectives and rules of procedure for the CVMP Pharmacovigilance Working Party (PhVWP-V)
2024 Annual Report on EudraVigilance for the European Parliament, the Council and the Commission
PSUSA/00000329/202407
Human medicines European public assessment report (EPAR): Sivextro, tedizolid phosphate, Date of authorisation: 23/03/2015, Revision: 25, Status: Authorised
Human medicines European public assessment report (EPAR): Scintimun, besilesomab, Date of authorisation: 11/01/2010, Revision: 8, Status: Authorised
EMA workshop on the challenges in drug development, regulation and clinical practice for immunoglobulins, Online, European Medicines Agency, Amsterdam, the Netherlands, from 5 March 2025, 14:00 (CET) to 5 March 2025, 18:00 (CET)
Certificates Processing System: Demo & Q&A session for industry stakeholders, Online, European Medicines Agency, Amsterdam, the Netherlands, from 13 March 2025, 12:30 (CET) to 13 March 2025, 13:00 (CET)
Minutes of the HMPC meeting 20-22 January 2025
EMA qualifies first artificial intelligence tool to diagnose inflammatory liver disease (MASH) in biopsy samples