What is the purpose of the EU Pharmaceuticals Directive?

The EU Pharmaceuticals Directive is a set of regulations that governs the production, distribution, and sale of pharmaceuticals within the European Union. The Directive has the aim of ensuring safety, efficacy, and quality of the medicines available to the public. It also sets out rules for the promotion and advertising of pharmaceuticals, as well as the control of prices. The Directive is made up of two parts: the Pharmaceuticals Directive and the Pharmaceuticals Regulation. The Directive describes the general principles of safety, efficacy, and quality of pharmaceuticals in the EU, while the Regulation sets out the more detailed rules that relate to manufacturing standards, clinical trials, data protection, and pricing. The main purpose of the EU Pharmaceuticals Directive is to protect public health and safety by regulating the production, distribution, sale, and use of medicines in the EU. It also seeks to create a more level playing field for pharmaceutical companies, helping to protect consumers from excessive prices and ensuring that medicines are available to those that need them. In addition, the Directive is designed to ensure that medicines meet the highest possible standards of safety, efficacy, and quality.

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What is the purpose of the EU Pharmaceuticals Directive?

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