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Commission Delegated Regulation (EU) 2016/161Dangos y teitl llawn

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)

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Changes over time for: Article 28

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There are currently no known outstanding effects by UK legislation for Commission Delegated Regulation (EU) 2016/161, Article 28. Help about Changes to Legislation

F1Article 28U.K.Obligations when supplying only part of a pack

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