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What is EMA Certification of Medicinal Products about?

This document provides information on the certification of medicinal products in the European Union. It discusses the different authorities that can authorize medicinal products in the EU/EEA, including the European Commission and national health authorities of EU member states. It also describes the different types of certificates that can be issued, including certificates for centrally authorized products by the European Medicines Agency (EMA) on behalf of the European Commission, and certificates under A

Author

Andrea Rojas

Language

EN