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The EMA is the EU agency responsible for evaluating and supervising medicines for humans and animals. Find information on medicines, events, news, FAQs and more on its homepage.
- European Union
The European Medicines Agency (EMA) protects and promotes...
- Medicines
The European Medicines Agency (EMA) facilitates development...
- About us
The European Medicines Agency (EMA) is a decentralised...
- European Union
The European Medicines Agency (EMA) facilitates development and access to medicines for countries within the European Union (EU). EMA evaluates applications for marketing authorisation submitted via the centralised procedure, monitors the safety of medicines across their lifecycle and provides information to healthcare professionals and patients.
The EMA 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.
EMA is a decentralised EU agency that evaluates, supervises and monitors medicines for public and animal health. Learn about EMA's mission, activities, organisation, history, careers, procurement, glossaries and more.
La EMA es la agencia descentralizada que evalúa y supervisa la seguridad de los medicamentos en la UE y el EEE. Conoce sus funciones, cometidos, beneficios y contacto en su web oficial.
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]
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).
