Animal testing ban conditions were resolved after a conflictive contact point between REACH regulation 1907/2006 and EU cosmetics regulation 1223/2009.
News
More Supervision on Notified Bodies by NEW 920/2013 Regulation
New EU implementing regulation 920/2013 to set more stringent requirements for the designation and supervision of Notified Bodies within Europe.
How to write cosmetic claims
Learn more from the experts at Obelis on how to write successful cosmetic claims for products on the EU market under regulation 655/2013.
ECORE Seminar by Obelis to be Launched at Cosmoprof North America
Obelis to launch ECORE Seminars at Cosmoprof North America to hold events concerning cosmetic regulations and Responsible Person requirements within Europe.
Obelis at Cosmoprof Bologna
Obelis to attend Cosoprof Worldwide Bologna, one of the world's largest beauty and cosmetics industry events. Meet our consultation team onsite.
Promotion & advertising rules for Medical Devices by EU Directives
Guidelines for advertising and promoting medical devices on the EU market as covered by directive 93/42/EEC. Ensure your product's compliance with Obelis.
Eucomed welcoming medical device proposals with reservations
EU medical technology association expresses its welcome to proposal of new medical device and in-vitro diagnostic regulations within Europe.
New Electronic Labeling for Medical Devices
Newly adopted EC regulation EU 207/2012 will introduce a new electronic labeling requirement for medical devices on the European market.
Ireland EU Presidency, to influence Medical Device Regulations
Ireland's 2013 EU presidency to set increased focus on requirements for notified bodies, medical device manufacturers, and authorized representatives.
Regulatory updates on the standard EN 980
More information on the previously missing EU standards EN 980 and EN ISO 15223-1. The Commission's intention was to have EN ISO 15225-1 replace EN 980.