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  1. The European Medicines Agency (EMA) is the EU agency responsible for evaluating and supervising medicines for humans and animals. Find information on centrally authorised medicines, latest news, events, FAQs and more.

  2. La Agencia Europea de Medicamentos (EMA) protege y promueve la salud humana y animal mediante la evaluación y el seguimiento de los medicamentos en la Unión Europea (UE) y el Espacio Económico Europeo (EEE). Qué hace. Los principales cometidos de la Agencia consisten en la autorización y el seguimiento de los medicamentos en la UE.

  3. The EMA is a decentralised agency that evaluates and monitors medicines for humans and animals in the EU and the EEA. It issues marketing authorisations, provides safety information, and supports research and development of new medicines.

  4. The European Medicines Agency (EMA) is an agency of the European Union (EU) in charge of the evaluation and supervision of pharmaceutical products. Prior to 2004, it was known as the European Agency for the Evaluation of Medicinal Products or European Medicines Evaluation Agency ( EMEA ).

  5. La Agencia Europea de Medicamentos (EMA, por sus siglas en inglés) es una agencia de la Comisión Europea descentralizada que se encarga de evaluar, autorizar, certificar y supervisar la comercialización de medicamentos que se comercialicen en la Unión Europea. [4]

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