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EMA is the EU agency responsible for evaluating and supervising medicines for humans and animals. Find information on medicines, clinical trials, events, news and more.
EMA is the EU agency that evaluates and monitors medicines for human and veterinary use. Find information on medicines authorised in the EU, their safety, side effects, shortages, 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.
EMA is the EU agency that evaluates and monitors medicines for humans and animals. It issues marketing authorisations, provides safety information and supports research and development of new medicines.
Jun 5, 2024 · EMA is the government agency that drives the advancement of Singapore's energy future. Learn about buying electricity, solar energy, statistics, proposals, grants and more on EMA's website.
Jun 6, 2024 · This website provides access to clinical data submitted by pharmaceutical companies to support their marketing applications for human medicines in the EU. The data include information on new medicines, COVID-19 vaccines and orphan 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 European Agency for the Evaluation of Medicinal Products or European Medicines Evaluation Agency ( EMEA ).
