European Medicines Agency (EMA) Find information on centrally authorised medicines Find all new and updated information published on our website in one place Find answers to the most frequent asked questions we receive PRAC carried out its broad range of responsibilities for managing the risks associated with medicine use
Medicines | European Medicines Agency (EMA) EMA evaluates applications for marketing authorisation submitted via the centralised procedure, monitors the safety of medicines across their lifecycle and provides information to healthcare professionals and patients
Apply - Step Up For Students EMA is Step Up For Students’ secure scholarship management platform—designed to make it easier for you to apply, upload documents and track your student’s scholarship journey all in one place
European Medicines Agency - Wikipedia The EMA was founded after more than seven years of negotiations among EU governments and replaced the Committee for Proprietary Medicinal Products and the Committee for Veterinary Medicinal Products, though both of these were reborn as the core scientific advisory committees
About us - European Medicines Agency (EMA) 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
What we do - European Medicines Agency (EMA) The European Medicines Agency (EMA) fosters scientific excellence in the evaluation and supervision of medicines This benefits public and animal health in the European Union (EU)
About EMA | Meet The Team Emergency Medical Associates is a physician-led, privately held physician management company that specializes in emergency and hospitalist medicine
European Medicines Agency – EMA | European Union 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 Economic Area (EEA)