What is the purpose of the EU Pharmaceuticals Directive?

The purpose of the EU Pharmaceuticals Directive is to ensure that all medicines sold in the European Union (EU) meet certain quality and safety standards. This directive provides a framework for the regulation of medicines that are sold within the EU. It regulates the manufacture, testing, safety and efficacy of all prescription and non-prescription medicines. The directive establishes a system of authorization and monitoring for all medicines that are authorized for sale within the European Union. It requires manufacturers and suppliers of medicines to comply with the European Union’s Good Manufacturing Practice (GMP) standards. The directive also sets out the quality and safety requirements for all individuals involved in the distribution of medicines within the EU. The Pharmaceuticals Directive is an important component of the European Union’s commitment to ensuring the safety of its citizens and the overall health of its population. The directive is also a critical tool for the protection of intellectual property rights and the promotion of research and innovation in the pharmaceutical sector. It is essential for improving public health and for ensuring public trust in pharmaceutical products.

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What is the purpose of the EU Pharmaceuticals Directive?

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