The Commission Q&A document has been updated

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.21)”.

The new version contains updated responses to Questions 1.1., 1.20., 1.21., and 2.21. - about safety features, replacing of safety features and using stickers to place the unique identifier.

Please read the Q&A document from here.