The European Medicines Agency works closely with the national competent authorities of the Member States of the European Union (EU) and the European Economic Area (EEA) responsible for medicinal products for human use.

The European Medicines Agency (EMA) works closely with the human and veterinary medicines regulatory authorities of the Member States of the European Union (EU) and the European Economic Area (EEA).

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 receive. Yearly updates to virus strains ensure vaccine effectiveness. Designation facilitates data sharing, promotes transparency and trust in clinical research.

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 Economic Area (EEA). The Agency's main responsibilities are authorising and monitoring medicines in the EU.

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). [4][5]

The EEA links the EU member states and three of the four EFTA states (Iceland, Liechtenstein, and Norway) into an internal market governed by the same EU laws. These rules aim to enable free movement of persons, goods, services, and capital within the European single market, including the freedom to choose residence in any country within this area.

Jul 4, 2023 · What Is the European Medicines Agency (EMA)? The European Medicines Agency (EMA) is a decentralized agency of the European Union (EU) whose goal is to promote and …

European Medicines Agency, 2021. Reproduction is authorised provided the source is acknowledged. (...*) Although they are not the official names for the Netherlands and the …

Jan 31, 2022 · Clinical trials in the EU and EEA are governed by the Clinical Trials Regulation (Regulation (EU) No 536/2014) which came into application on 31 January 2022. It is part of a broad initiative to transform the EU/EEA clinical trials environment in support of large clinical trials in multiple European countries, to the benefit of medical ...

Nov 2, 2023 · What Is the European Economic Area (EEA) Agreement? The European Economic Area (EEA) Agreement is an agreement made in 1992 that brought the European Union (EU) …