Directive 2001/83/EC of the European Parliament and of the… Article 47

Article 47

The principles and guidelines of good manufacturing practices for medicinal products referred to in Article 46(f) shall be adopted in the form of a directive, in accordance with the procedure referred to in Article 121(2). Detailed guidelines in line with those principles will be published by the Commission and revised necessary to take account of technical and scientific progress.

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CitationArticle 47 of Directive 2001/83/EC of the European Parliament and of the… (LawPlayer, data as of 2026-07-04)

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