European Medicines Agency (EMA) | Website analytics by TrustRadar
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ema.europa.eu Health Medicine Regulation European Union Government

European Medicines Agency (EMA)

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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Founded in

1995

Supported Languages

English, etc

Website Key Features

Medicine Evaluation

Scientific evaluation of medicines for human and veterinary use within the EU.

Safety Monitoring

Continuous monitoring of the safety of medicines through pharmacovigilance activities.

Scientific Advice

Providing scientific advice to pharmaceutical companies on the development of medicines.

Public Health

Contributing to the protection and promotion of public and animal health.

Regulatory Guidance

Offering guidance on regulatory procedures and requirements for medicines.

Collaboration

Collaborating with national competent authorities, international partners, and stakeholders.

Transparency

Ensuring transparency in the regulatory process through public access to documents and data.

Innovation

Supporting innovation in medicine development to address unmet medical needs.

Additional information

Headquarters

Amsterdam, the Netherlands

Key People

Executive Director: Emer Cooke

Parent Organization

European Union

Website

https://www.ema.europa.eu

Legal Framework

Regulation (EC) No 726/2004

Mission

To foster scientific excellence in the evaluation and supervision of medicines, for the benefit of public and animal health in the EU.

Vision

To be the leading authority in the regulation of medicines, recognized for its scientific expertise, independence, and commitment to public health.

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