What is the purpose of the EU Pharmaceuticals Directive?

The purpose of the EU Pharmaceuticals Directive is to ensure that medications sold in the European Union meet the highest standards of safety, quality, and efficacy. This directive also sets out principles and guidelines for the production, distribution, and sale of pharmaceutical products in order to protect the public. The directive includes specific requirements for pharmaceutical companies to be aware of when manufacturing, marketing, distributing, and selling drugs. The directive also implements strict safety and efficacy requirements for medication manufacturers to help protect patients and the healthcare system from unsafe treatments. This includes limits on the amount of active ingredients that can be included in a medication, as well as labeling requirements so that medications are easy to identify and understand. The directive also provides incentives for companies to invest in the development of new and improved treatments. The directive requires that pharmaceutical companies invest a certain percentage of their revenue in research and development, thus promoting scientific innovation. In Washington, the Washington Board of Pharmacy regulates the sale and distribution of pharmaceuticals—which means that all companies selling medications must adhere to the EU Pharmaceuticals Directive. This ensures that Washington patients receive high-quality treatments that are safe and effective.

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