The European Commission released updated Q&A document regarding Safety Features for Medicinal Products for Human Use
The European Commission has released an updated Q&A document regarding the Delegated regulation on Safety Features for Medicinal Products for Human Use. Changes were made to four answers: 1.8., 1.14., 2.14 and 4.4.
In addition, four new questions with answers were added to the document. The new questions are 4.6., 5.12., 5.13. and 6.9.
The revised document can be found here: