EU Council report shows progress on proposed new medical device and in-vitro diagnostic device regulations to replace previous European directives.

EU Council report shows progress on proposed new medical device and in-vitro diagnostic device regulations to replace previous European directives.
Representatives from Obelis' European Responsible Person Center and EU regulatory team will be attending Cosmoprof Asia from November 12-14, 2014.
Useful information on differentiation and classification of medical devices and cosmetic products intended for use on the EU market. Learn more with Obelis.
European regulatory and compliance experts Obelis announce new formula verification service for manufacturers starting the EU compliance process.
EU regulatory experts and Responsible Person service provider Obelis joins Personal Care Product Council (PCPC) as an Internal Associate from July 2014.
Learn more about good manufacturing practices for cosmetic manufacturers operating with sub-contractors within Europe. Talk to Obelis' EU regulatory experts.
From July 2014, the national Irish medical and cosmetics regulator, Health Products Regulatory Authority, will become known as the Irish Medicines Board.
Read more about the Cosmetics Products Notification Portal created under EU cosmetics regulation 1223/2009/EC to replace national registration and notification.
New EC guidelines detail relevant data to be considered as minimum when detailing a Product Information File for cosmetic products on the EU market.
Animal testing ban conditions were resolved after a conflictive contact point between REACH regulation 1907/2006 and EU cosmetics regulation 1223/2009.