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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). What it does. The Agency's main responsibilities are authorising and monitoring medicines in the EU.
About us. About this website. The European Medicines Agency's (EMA) corporate website is EMA's main communication channel. Information in this section helps you get the most out of its special features such as the search and glossaries of medical and regulatory terms. Page contents. In this section. Related content.
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 ).
EMA is the first regulatory authority worldwide to provide such broad access to clinical data. For more information on the clinical data on this website, see Clinical data available. For more information on EMA and its policy on the publication of clinical data, see the EMA corporate website. Latest news.
Jul 4, 2023 · The European Medicines Agency (EMA) is a decentralized agency of the European Union (EU) whose goal is to promote and protect human and animal health. The EMA is the European Union’s equivalent...
23 hours ago · The EMA collaborates closely with its EU partners through the European regulatory network, which allows for the exchange of information and coordination of efforts to address common challenges. This network enhances the capacity to identify and respond to potential risks associated with substandard or falsified drugs. EMA's Role in Quality ...
The European Medicines Agency (EMA) is a decentralised agency of the European Union (EU) responsible for the scientific evaluation, supervision and safety monitoring of medicines in the EU. EMA is governed by an independent Management Board. Its day-to-day operations are carried out by the EMA staff, overseen by EMA's Executive Director.
