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Outcomes of the Committee for Veterinary Medicinal Products (CVMP) meeting.
EMA and the European Commission’s Directorate-General for Health and Food Safety (DG SANTE) have signed a working arrangement with the Ministry of Food and Drug Safety (MFDS) of the Republic of Korea for the exchange of confidential information on medical and medicinal products.
EMA’s human medicines committee (CHMP) recommended eight medicines for approval at its April 2024 meeting.
EMA has published a number of recommendations to address vulnerabilities in the production and delivery of medicines included in the Union list of critical medicines and strengthen their supply chain.
Report on COVID-19 vaccine strain updates: global regulators agree on timing and data requirements
GLP-1 receptor agonists: available evidence not supporting link with suicidal and self-injurious thoughts and actions
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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...