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
Start date: 13 May 2024
End date: 17 May 2024
EventHumanClinical trials
Clinical Trials Information System (CTIS): Walk-in clinic - May 2024

This walk-in clinic on CTIS functionalities provides an opportunity for sponsors to receive practical information about the Clinical Trials Information System by asking questions to CTIS experts in real time.

Online
European Medicines Agency, Amsterdam, the Netherlands
Live Broadcast
Start date: 15 May 2024, 16:00 (CEST)
End date: 15 May 2024, 17:00 (CEST)
EventHumanClinical trials