The European Commission released updated Q&A document regarding Safety Features for Medicinal Products for Human Use

The European Commission has published a new version of the Questions & Answers document on “Safety Features for Medicinal Products for Human Use (V.19)”. A new Q&A (1.29) was added and Q&As 1.22, 5.8 and 7.19 were revisioned. 

The revised document can be found here (modifications from the previous version have been highlighted): 

The document is also available on EMVO’s website in the Knowledge Database section – Documents Overview.