Commission Delegated Regulations (EU) 2016/161

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

At the momment, our goal is to target at pharmaceutical companies by taking advantage of European Union Regulation 2016/161, which requires the use of a unique identifier for medicinal products by the end of February 2019,

(a) ‘unique identifier’ means the safety feature enabling the verification of the authenticity and the
identification of an individual pack of a medicinal product 

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