Events

Multi-stakeholder webinar on the HMA-EMA Catalogues of real-world data sources and studies

This event provides an overview of the HMA-EMA Catalogues of real-world data sources and studies including their benefits and significance in regulatory practices.

Online
European Medicines Agency, Amsterdam, the Netherlands
Live broadcast
Alguskuupäev: 4 märts 2024, 10:00 (CET)
Lõpu kuupäev: 4 märts 2024, 12:00 (CET)
EventHumanData on medicines
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
Alguskuupäev: 4 märts 2024
Lõpu kuupäev: 8 märts 2024
EventHumanClinical trials