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Find information on centrally authorised medicines. Find all new and updated information published on our website in one place. Find answers to the most frequent asked questions we …

The European Medicines Agency (EMA) facilitates development and access to medicines for countries within the European Union (EU). EMA evaluates applications for marketing …

The European Medicines Agency (EMA) protects and promotes human and animal health by evaluating and monitoring medicines within the European Union (EU) and the European …

L’Agence européenne des médicaments (EMA) contribue à protéger et à promouvoir la santé humaine et animale en évaluant et en contrôlant les médicaments au sein de l’Union …

欧洲药品管理局（ema）负责在泛欧洲范围内，评估和监督药品的集中上市许可（cap），是制定全球药品监管标准的重要力量。 受英国脱欧影响，原本设置在伦敦的EMA已于2019年3月迁 …

The European Medicines Agency (EMA) operates as a decentralised scientific agency (as opposed to a regulatory authority) of the European Union (EU) and its main responsibility is …

The national medicine registers in the different Member States of the European Union (EU) and European Economic Area (EEA) contain information on medicines authorised in those …

Penser l’objet, utilitaire ou décoratif, rechercher la forme, la texture, imaginer sa couleur, envisager le processus de fabrication, expérimenter, faire des choix sont autant d’étapes qui …

The European Medicines Agency (EMA) is an agency of the European Union. It manages the evaluation and quality of pharmaceutical products. It started in 1995. The idea was to make it …