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
Datum začátku: 31 Březen 2025
Datum konce: 4 Duben 2025
Event Human Clinical trials
Twelfth Industry Standing Group (ISG) meeting
Online
European Medicines Agency, Amsterdam, the Netherlands
Datum začátku: 28 Březen 2025, 09:00 (CET)
Datum konce: 28 Březen 2025, 14:00 (CET)
Event Human Corporate
Quarterly System Demo - Q1 2025
Online
European Medicines Agency, Amsterdam, the Netherlands
Live broadcast
Datum začátku: 26 Březen 2025, 09:00 (CET)
Datum konce: 26 Březen 2025, 11:30 (CET)
Event Corporate
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