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Information for you. Featured news and updates for patients and carers. Featured news and updates for healthcare professionals, including doctors, nurses and pharmacists. Featured news and updates for animal health professionals and users of veterinary medicines such as pet owners.
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 ...
The European Medicines Agency (EMA) is a decentralised agency of the European Union (EU). It is responsible for the scientific evaluation, supervision and safety monitoring of medicines.
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.
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).
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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).
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Mar 1, 2022 · Details. Publication date. 1 March 2022. Author. Directorate-General for Health and Food Safety.
What’s new. Find all new and updated information published on our website in one place below. Filters are available to narrow results down based on your interests, such as whether it relates to human or veterinary medicines or specific topics. This overview covers up to two months back. Current month Previous month Two months ago.
