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  1. EMA is the EU agency responsible for evaluating and supervising medicines for humans and animals. Find information on medicines, events, news and FAQs on its website.

    • Medicines

      The European Medicines Agency (EMA) facilitates development...

    • What's New

      What’s new. Find all new and updated information published...

    • About This Website

      The European Medicines Agency's (EMA) corporate website is...

    • What We Do

      The mission of the European Medicines Agency (EMA) is to...

  2. 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.

  3. Find the latest updates on human and veterinary medicines, events, documents and guidance from the EMA. Filter by date, content status and topic to narrow your search results.

    • Overview
    • What It Does
    • Who Benefits
    Role: EMA guarantees the scientific evaluation, supervision & safety monitoring of human & veterinary medicines in the EU.
    Executive Director: Emer Cooke
    Established in: 1995
    Number of staff:897

    The Agency's main responsibilities are authorising and monitoring medicines in the EU. Companies apply to it for a single marketing authorisation, which is issued by the European Commission. If granted, this enables them to market the medicine concerned throughout the EU and the EEA. Given the wide-ranging scope of the centralised procedure, most g...

    The EMA's work benefits: 1. patients 2. healthcare professionals 3. academics 4. pharmaceutical companies 5. medicine developers 6. health policymakers Through its scientific guidelines, scientific advice programme and incentives, it facilitates research into new medicines and encourages development, thereby translating progress in medical science ...

  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 ).

  5. 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.

  6. Jun 6, 2024 · 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.

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