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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: 15 April 2024
End date: 19 April 2024
Event Human Clinical trials
SPOR status update

EMA is organising a public webinar on Substance, Product, Organisation, Referentials (SPOR) Regulatory Data Management (RDM) services status update.

Online
European Medicines Agency, Amsterdam, the Netherlands
Live broadcast
Start date: 10 April 2024, 10:00 (CEST)
End date: 10 April 2024, 12:30 (CEST)
Event Human Medicines
Cancer Medicines Forum workshop: April 2024
Online
European Medicines Agency, Amsterdam, the Netherlands
Live broadcast
Start date: 5 April 2024, 13:00 (CEST)
End date: 5 April 2024, 18:00 (CEST)
Event Human Medicines
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