The European Medicines Agency is a decentralised agency of the European Union responsible for the evaluation, supervision and safety monitoring of medicines.
The European Medicines Agency (EMA) is a decentralized agency of the European Union (EU) responsible for the scientific evaluation, supervision, and safety monitoring of medicines in the EU. EMA plays a vital role in ensuring that all medicines available on the EU market are safe, effective, and of high quality. The agency serves as a hub for scientific excellence in the regulation of medicines, bringing together experts from across Europe to assess and monitor medicines.
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Scientific evaluation of medicines for human and veterinary use within the EU.
Continuous monitoring of the safety of medicines through pharmacovigilance activities.
Providing scientific advice to pharmaceutical companies on the development of medicines.
Contributing to the protection and promotion of public and animal health.
Offering guidance on regulatory procedures and requirements for medicines.
Collaborating with national competent authorities, international partners, and stakeholders.
Ensuring transparency in the regulatory process through public access to documents and data.
Supporting innovation in medicine development to address unmet medical needs.
Amsterdam, the Netherlands
Executive Director: Emer Cooke
European Union
https://www.ema.europa.eu
Regulation (EC) No 726/2004
To foster scientific excellence in the evaluation and supervision of medicines, for the benefit of public and animal health in the EU.
To be the leading authority in the regulation of medicines, recognized for its scientific expertise, independence, and commitment to public health.
Security headers report is a very important part of user data protection. Learn more about http headers for ema.europa.eu