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: 4 Listopad 2024
Datum konce: 8 Listopad 2024
Event Human Clinical trials
Biannual Big Data Steering Group and industry stakeholders meeting - Oct 2024

The meeting was held in the context of EMA’s continuous endeavours to foster regular interactions with industry stakeholders on topics of common interest, and in this instance, big data.

Online
European Medicines Agency, Amsterdam, the Netherlands
Datum začátku: 25 Říjen 2024, 09:00 (CEST)
Datum konce: 25 Říjen 2024, 11:00 (CEST)
Event Human Veterinary Data on medicines
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