European Medicines Agency pre-authorisation procedural advice for users of the centralised procedure
European Medicines Agency pre-authorisation procedural advice for users of the centralised procedure
European Medicines Agency pre-authorisation procedural advice for users of the centralised procedure
PSUSA/00002849/202411
Global IDMP Working Group (GIDWG) Stakeholder Meeting: 1-3 October 2025, European Medicines Agency, Amsterdam, the Netherlands, Broadcast, from 3 October 2025, 12:30 (CEST) to 3 October 2025, 14:00 (CEST)
GIDWG Stakeholder Meeting: 1-3 October 2025, European Medicines Agency, Amsterdam, the Netherlands, Broadcast, from 3 October 2025, 12:30 (CEST) to 3 October 2025, 14:00 (CEST)
PSUSA/00003162/202501
Human medicines European public assessment report (EPAR): Sunosi, solriamfetol, Date of authorisation: 16/01/2020, Revision: 10, Status: Authorised
Medicine shortage communication (MSC): Victoza 6 mg/mL solution for injection in pre-filled pen (liraglutide)
Veterinary medicines European public assessment report (EPAR): Equilis StrepE, live vaccine against Streptococcus equi, Status: Authorised
Veterinary medicines European public assessment report (EPAR): Enteroporc Coli AC, neonatal piglet colibacillosis (recombinant, inactivated),Clostridium perfringens vaccine (inactivated), Status: Authorised
Veterinary medicines European public assessment report (EPAR): Emdocam, meloxicam, Status: Authorised