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2 de jun. de 2015 · EMA is the EU agency responsible for the evaluation and supervision of medicines for human and veterinary use. Find information on medicines, events, news, FAQs and more.
- Medicines
The European Medicines Agency (EMA) facilitates development...
- Marketing authorisation
The European Medicines Agency (EMA) is responsible for the...
- What We Do
The mission of the European Medicines Agency (EMA) is to...
- Who We Are
The European Medicines Agency (EMA) is a decentralised...
- About us
The European Medicines Agency (EMA) is a decentralised...
- What's New
What’s new. Find all new and updated information published...
- Search
Highly pathogenic avian influenza is a serious threat to...
- Scientific guidelines
The European Medicines Agency's Committee for Medicinal...
- Medicines
EMA is the EU agency that evaluates and monitors medicines for human and veterinary use. Find information on medicines authorised in the EU, their safety, side effects, shortages, and more.
ema es una entidad privada que acredita a los organismos de evaluación de la conformidad en México. Conoce sus servicios, reconocimientos, eventos y contacto en su portal oficial.
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.
EMA is the EU agency that evaluates and monitors medicines for humans and animals. It issues marketing authorisations, provides safety information and supports research and development of new medicines.
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 responsible for the scientific evaluation of centralised marketing authorisation applications (MAA). Once granted by the European Commission, the centralised marketing authorisation is valid in all European Union (EU) Member States, Iceland, Norway and Liechtenstein. Human Regulatory and procedural guidance.
