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Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use. The Directive dealt with the disparities between certain national provisions, in particular between provisions relating to medicinal products, which directly affected the functioning of the internal market of the European Union.
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|This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Directive_2001/83/EC". A list of authors is available in Wikipedia.|