The European Commission has published the revised version of the Guideline on the Packaging Information of Medicinal Products for Human Use
07.08.2013
The Agency for Medicinal Products and Medical Devices (HALMED) informs marketing authorisation holders that the European Commission has published the revised version of the Guideline on the Packaging Information of Medicinal Products for Human Use Authorised by the EU. The Guideline includes also the Croatian requirements related to the "Blue box” that came in effect as of 1st July 2013.
The Guideline on the Packaging Information of Medicinal Products for Human Use Authorised by the EU is available on the web pages of the European Commission or here.
