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) facilitates development and access to medicines for countries within the European Union (EU). EMA evaluates applications for marketing …

The European Medicines Agency (EMA) protects and promotes human and animal health by evaluating and monitoring medicines within the European Union (EU) and the European …

The European Medicines Agency (EMA) is a decentralised agency of the European Union (EU). It is responsible for the scientific evaluation, supervision and safety monitoring of medicines.

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 …

The mission of the European Medicines Agency (EMA) is to foster scientific excellence in the evaluation and supervision of medicines, for the benefit of public and animal health in the …

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.

1 day ago · The EMA recommends all sponsors to verify if their trials comply with the Guidance on results postings through looking for their sponsor name in EU CTR. To learn how to post …

These three words signify the mission of EMA: to make science-based decisions, to regulate medicines, and to promote human and animal health. EMA has a similar role as FDA in the …

3 days ago · Adopted Commission Decisions of the last six months Last updated on 28/01/2025.Union Register of medicinal products