Glatiramer acetate
Glatiramer acetate
Glatiramer acetate
Human medicines European public assessment report (EPAR): Intelence, etravirine, Date of authorisation: 28/08/2008, Revision: 31, Status: Authorised
European Union example instances - E2B(R3) testing files
Test cases (1a-10) RTFs
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)