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To ensure high standards of quality and safety on Pharmaceutical products, the EU has put in place a comprehensive legal framework. The EU also promotes the internal market with actions to stimulate innovation and facilitate free movement.

The EU has a European Medicines Agency which, while leaving each member country the authority to place a new drug on the market, issues an authoritative scientific opinion.​
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Medicinal products
Committee and expert groups
European Medicines Agency
EU Register of medicines