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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.
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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.
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.
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Role: EMA guarantees the scientific evaluation, supervision & safety monitoring of human & veterinary medicines in the EU.Executive Director: Emer CookeEstablished in: 1995Number of staff:897The 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.
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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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.