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Factsheet – 30 years of medicines in the EU

Since 1995, the European Commission has authorised the marketing of medicines across the whole European Union. Central authorisations are valid in all EU Member States and are based on rigorous scientific evaluations by the European Medicines Agency, which gathers experts from all Member States. A new medicine authorisation is only granted if the required quality, safety and efficacy standards are met.

Read the factsheet published by EC Directorate-General for Health and Food Safety on 19 October 2025.


OpenEdition vous propose de citer ce billet de la manière suivante :
lsgilbert (25 novembre 2025). Factsheet – 30 years of medicines in the EU. ELSIBI. Consulté le 16 mars 2026 à l’adresse https://doi.org/10.58079/157h8


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