Vendor registration in the EudraVigilance external compliance testing environment (XCOMP) - Registration procedure
EudraVigilance user declaration for qualified person for pharmacovigilance/responsible person for EudraVigilance
New Organization First User QPPV/RP or Change of EU QPPV/RP
EudraVigilance registration documents
IRIS guide for applicants - How to create and submit scientific applications, for industry and individual applicants
First EMA-Animal Health Europe annual bilateral meeting July 2024, Online, European Medicines Agency, Amsterdam, the Netherlands, from 1 July 2024, 13:30 (CEST) to 1 July 2024, 15:00 (CEST)
Highlights - First EMA-Animal Health Europe annual bilateral meeting July 2024
Final minutes – HMA-EMA joint Big Data Steering Group teleconference from 27 May 2024
EMA is closed on Assumption Day, 15 August
Human medicines European public assessment report (EPAR): Dabigatran Etexilate Accord, dabigatran etexilate, Date of authorisation: 26/05/2023, Revision: 2, Status: Authorised