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EMA is hosting the fourteenth industry stakeholder platform on the operation of the centralised procedure for human medicines on 23 June 2025.
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...