What is the purpose of the EU Pharmaceuticals Directive?

The EU Pharmaceuticals Directive is a set of regulations that applies to the manufacturing, distribution, and sale of medicines within the European Union (EU). The purpose of the directive is to protect the public by ensuring that medicines provided within the EU meet the highest standards of safety, quality, and efficacy. This directive is also designed to ensure that all products comply with the principles of good manufacturing practice and the requirements of the EU code of good distribution practices. It also helps to ensure that medicines are only sold in locations where they can be properly monitored and controlled to prevent misuse. In addition, the directive helps protect the intellectual property rights of manufacturers and distributors by preventing the unauthorized sale or export of medicines outside of the EU. Furthermore, it helps promote fair competition, transparency, and affordability for consumers. Finally, it helps to strengthen the EU’s role in the global pharmaceutical industry by reducing the risk of counterfeit medicines entering the European market.

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What is the purpose of the EU Pharmaceuticals Directive?

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