Events

Sixth European Medicines Agency (EMA) and EFPIA bilateral meeting

EMA and EFPIA met in the context of EMA's annual bilateral meetings with industry stakeholder organisations

European Medicines Agency, Amsterdam, the Netherlands
Aloituspäivämäärä: 6 helmikuu 2024
Lopetuspäivämäärä: 6 helmikuu 2024
EventHumanMedicines
Pharmacovigilance Risk Assessment Committee (PRAC): 5-8 February 2024

The Pharmacovigilance Risk Assessment Committee (PRAC) is the committee that is responsible for assessing all aspects of the risk management of medicines for human use.

European Medicines Agency, Amsterdam, the Netherlands
Aloituspäivämäärä: 5 helmikuu 2024
Lopetuspäivämäärä: 8 helmikuu 2024
EventHumanPharmacovigilance
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
Aloituspäivämäärä: 29 tammikuu 2024
Lopetuspäivämäärä: 2 helmikuu 2024
Event