Events

Mandatory use of ISO/ICH E2B(R3) individual case safety reporting in the EU: hands-on training course using the EudraVigilance system

EudraVigilance is the EU's system for managing and analysing information on adverse reactions to medicines which have been authorised or are being studied in clinical trials in the European Economic Area (EEA) and supports the reporting and analysis of suspected adverse reactions originating from clinical trials and the post-authorisation phase of...

Online
Aloituspäivämäärä: 13 toukokuu 2024
Lopetuspäivämäärä: 17 toukokuu 2024
EventHumanClinical trials
DARWIN EU Advisory Board meeting: 3 May 2024
Online
European Medicines Agency, Amsterdam, the Netherlands
Aloituspäivämäärä: 3 toukokuu 2024, 13:00 (CEST)
Lopetuspäivämäärä: 3 toukokuu 2024, 14:30 (CEST)
EventCorporateData on medicines
EMA traineeship programme informative session (2024)

Join this information session and learn how to apply to the EMA traineeship

Online
European Medicines Agency, Amsterdam, the Netherlands
Live broadcast
Aloituspäivämäärä: 23 huhtikuu 2024, 10:00 (CEST)
Lopetuspäivämäärä: 23 huhtikuu 2024, 11:00 (CEST)
EventCorporateCareers