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Euro­pean Com­mis­si­on Q&A Ver­si­on 20

The European Commission has published a new version of the Questions & Answers (Q&A) document on "Safety features for medicinal products for human use (V.20)". New is question 5.14: Is it allowed to verify the authenticity of the UI when the product is not in physical possession? The document can...
The Euro­pean Com­mis­si­on has published a new ver­si­on of the Ques­ti­ons & Ans­wers (Q&A) docu­ment on “Safe­ty fea­tures for medi­cinal pro­ducts for human use (V.20)”. New is ques­ti­on 5.14: Is it allo­wed to veri­fy the authen­ti­ci­ty of the UI when the pro­duct is not in phy­si­cal pos­ses­si­on? The docu­ment can be found on the web­site of the EU Com­mis­si­on.

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