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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)
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Article 20Verification of the authenticity of the unique identifier by wholesalers
A wholesaler shall verify the authenticity of the unique identifier of at least the following medicinal products in his physical possession:
(a)
medicinal products returned to him by persons authorised or entitled to supply medicinal products to the public or by another wholesaler;
(b)
medicinal products he receives from a wholesaler who is neither the manufacturer nor the wholesaler holding the marketing authorisation nor a wholesaler who is designated by the marketing authorisation holder, by means of a written contract, to store and distribute the products covered by his marketing authorisation on his behalf.
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