Events


Event Corporate

The ERA-DG together with additional technical experts from the EU network is hosting a stakeholder webinar for industry and contract research organisations (CROs) on the revised ERA guideline for human medicinal products.

Event Human

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...

Event Human Clinical trials