EU Member States - European Medicines Agency (EMA)
WEBThe 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 Economic Area (EEA).
European Medicines Agency (EMA)
WEBFeatured news and updated for European Academics and researchers in the field of medicine development. The European Medicines Agency is a decentralised agency of the European Union responsible for the evaluation, supervision and safety monitoring of …
National competent authorities - European Medicines Agency …
WEBThe 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) responsible for human medicines.
European Medicines Agency - Wikipedia
WEBThe Agency decentralises its scientific assessment of medicines by working through a network of about 4500 experts throughout the EU. The EMA draws on resources of over 40 National Competent Authorities (NCAs) of EU Member states.
European Medicines Agency – EMA | European Union
WEBThe 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). What it does. The Agency's main responsibilities are authorising and monitoring medicines in the EU.
Health Union: a stronger role for the European Medicines Agency
WEBJan 20, 2022 · The European Medicines Agency (EMA) will be better equipped to monitor and mitigate shortages of medicinal products and medical devices considered to be critical in order to address public health emergencies.
WEBEU UNION REGISTER OF MEDICINAL PRODUCTS. - . FREQUENTLY ASKED QUESTIONS. The purpose of these FAQ’s is to provide an overview on issues that have been frequently raised by the public in the context of the EU Union Register of …
NATIONAL CONTACTS - Heads of Medicines Agencies
WEBHeads of Medicines Agencies: National Contacts. You are here: Home. > Human Medicines. > National Contacts. Select country. For the United Kingdom, as of 1 January 2021, European Union law applies only to the territory of Northern Ireland (NI) to the extent foreseen in the Protocol on Ireland / NI.
Heads of Medicines Agencies: About HMA
WEBThe Heads of Medicines Agencies (HMA) is a network of the heads of the National Competent Authorities (NCA) whose organisations are responsible for the regulation of medicinal products for human and veterinary use in the European Economic Area.
The European Medicines Agency's EU conditional marketing authorisations ...
WEBJan 30, 2021 · EU member states could have opted for emergency use in their own territory but have chosen a more robust, unified EU approach, with a joint assessment benefiting all member states and prioritising citizens' safety across Europe equally.