Commission Delegated Regulation (EU) 2016/161Show full title

Commission Delegated Regulation (EU) 2016/161 of 2 October 2015 supplementing Directive 2001/83/EC of the European Parliament and of the Council by laying down detailed rules for the safety features appearing on the packaging of medicinal products for human use (Text with EEA relevance) (revoked)

F1Article 49U.K.Application in Member States with existing systems for the verification of the authenticity of medicinal products and for the identification of individual packs

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Textual Amendments applied to the whole legislation