International Electrotechnical Commission introduce 4th edition of IEC 6061-1-2:2004 to include technical revisions on risk analysis and immunity requirements.
News
ISO 9001:2015 – What You Need to Know
Find out more about ISO 9001:2015 – why it is coming into effect, what impact it may have for your products, transition periods, and how to prepare for it.
EC Guidelines on Product Information File
New EC guidelines detail relevant data to be considered as minimum when detailing a Product Information File for cosmetic products on the EU market.
Cosmetics animal testing ban conflict with REACH is solved
Animal testing ban conditions were resolved after a conflictive contact point between REACH regulation 1907/2006 and EU cosmetics regulation 1223/2009.
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.