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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: CHAPTER XI

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

F1CHAPTER XIU.K.TRANSITIONAL MEASURES AND ENTRY INTO FORCE

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