The new version of the EC Questions & Answers document answers about verification when product is not in physical possession

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)”.

It answers if is it allowed to verify the authenticity of the UI when the product is not in physical possession. EC explains - yes, but only as an additional check to Article 20 of Commission Delegate Regulation 2016/161.

The document is available on EMVO’s website in the Knowledge Database section.

The modifications from the previous version have been highlighted for your convenience and includes the addition of a new Q&A (5.14).