
National competent authorities - European Medicines Agency (EMA)
The European Medicines Agency works closely with the national competent authorities of the Member States of the European Union (EU) and the European Economic Area (EEA) …
EU Member States - European Medicines Agency (EMA)
The European Medicines Agency (EMA) works closely with the human and veterinary medicines regulatory authorities of the Member States of the European Union (EU) and the European …
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 …
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 …
European Medicines Agency - Wikipedia
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 Economic Area - Wikipedia
The European Economic Area (EEA) was established via the Agreement on the European Economic Area, [4] an international agreement which enables the extension of the European …
European Medicines Agency, 2021. Reproduction is authorised provided the source is acknowledged. (...*) Although they are not the official names for the Netherlands and the …
European Medicines Agency (EMA): Meaning and Examples - Investopedia
Jul 4, 2023 · What Is the European Medicines Agency (EMA)? The European Medicines Agency (EMA) is a decentralized agency of the European Union (EU) whose goal is to promote and …
What Is the European Economic Area (EEA) Agreement? - Investopedia
Nov 2, 2023 · What Is the European Economic Area (EEA) Agreement? The European Economic Area (EEA) Agreement is an agreement made in 1992 that brought the European Union (EU) …
• Scientific assessment of all innovative medicines for authorisation throughout the EEA One application, one evaluation, one authorisation valid everywhere in Europe e.g. for cancer, …