Access to documents
Access to documents
Access to documents
How to prepare and review a summary of product characteristics
ACT EU workshop on multiplicity in confirmatory clinical trials: From two-arm to platform trials , Online, European Medicines Agency, Amsterdam, the Netherlands, Broadcast, from 27 November 2026, 09:00 (CET) to 27 November 2026, 15:00 (CET)
Timetable: Safety signal - Assessment of responses to request for supplementary information (RSI)
Second ACT EU webinar on contractual agreements , Online, European Medicines Agency, Amsterdam, the Netherlands, from 7 December 2026, 10:00 (CET) to 7 December 2026, 15:00 (CET)
Records of data processing activity for the declaration of gainful employment of staff members’ spouses and registered partners
Recommended submission dates for veterinary medicinal products
Agenda - European Medicines Agency workshop on bacteriophage therapy
Records of data processing activity for the engagement in active senior initiative
List of clinical evaluation consultation procedure (CECP) opinions issued for medical devices awaiting finalisation of conformity assessment