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  1. The EMA is the EU agency responsible for evaluating and supervising medicines for human and veterinary use. Find information on medicines, clinical trials, events, news and more on its website.

    • Medicines

      Our Medicine finder above helps you find information on...

    • About us

      The European Medicines Agency (EMA) is a decentralised...

    • 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...

    • Who We Are

      The European Medicines Agency (EMA) is a decentralised...

    • Marketing Authorisation

      The European Medicines Agency (EMA) is responsible for the...

    • What's New

      Find all new and updated information published on our...

  2. EMA is the EU agency that evaluates and monitors medicines for human and veterinary use. Find information on medicines authorised by EMA, national registers, therapeutic areas, medicine shortages, COVID-19 medicines and more.

  3. EMA is a decentralised EU agency that evaluates, supervises and monitors medicines for public and animal health. Learn about EMA's mission, activities, organisation, history, careers, procurement, glossaries and more.

  4. EMA is the government agency that drives the advancement of Singapore's energy future. Find out more about buying electricity, applying for licences, installing solar, proposals and grants, and joining EMA.

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    • Overview
    • What It Does
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    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 ...

    EMA is the EU agency that evaluates and monitors medicines for humans and animals. Visit its website to learn more about its role, responsibilities, partners, publications and careers.

  5. 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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  7. This website supports the running of clinical trials for human medicines in the EU and EEA, and provides information on authorised trials. It is based on the Clinical Trials Regulation, which aims to streamline and harmonise the processes for clinical trials across the region.