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The European Medicines Agency's (EMA) office is closed on Thursday 15 August 2024.
Free advice and guidance available for manufacturers and notified bodies
Validating processes is an important step towards establishment of African Medicines Agency
14 new medicines recommended for approval; another 11 medicines recommended for extension of therapeutic indications
Outcomes of the Committee for Veterinary Medicinal Products (CVMP) meeting.
PRAC elects new chair
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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...