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 Economic Area (EEA).
The medicines regulatory authorities of the Member States, or 'national competent authorities', are responsible for the authorisation of medicines available in the EU that do not pass though the centralised procedure.
This unique collaborative model, knows as the European medicines regulatory network, enables Member States to pool resources and coordinate work to regulate medicines efficiently and effectively.
The Member States are also represented in EMA's Management Board.
- National competent authorities (human)
- National competent authorities (veterinary)
- Heads of Medicines Agencies
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