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Brochure: The European regulatory system for medicines

November 11, 2016

The European Medicines Agency developed a brochure on the European regulatory system for medicines.

The booklet explains how the European regulatory system for medicines operates. It describes how medicines are authorized and monitored in the European Union (EU) and how the European medicines regulatory network – a partnership between the European Commission, the medicines regulatory authorities in EU Member States and the European Economic Area (EEA), and the European Medicines Agency (EMA) – works to ensure that patients in the EU have access to high-quality, effective and safe medicines.

The brochure can be downloaded here:

The European regulatory system for medicines

Original Article