European Medicines Agency publishes booklet on European regulatory system for medicines
The European Medicines Agency (EMA) today published an illustrated leaflet explaining how the European regulatory system for medicines operates. It describes how medicines are authorised and monitored in the European Union (EU) and how the European medicines regulatory network – a partnership between the European Commission, the 50 medicines regulatory authorities in the EU and the European Economic Area (EEA), and the EMA – works to ensure that patients in the EU have access to safe and effective medicines.
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