Learn more from the experts at Obelis on how to write successful cosmetic claims for products on the EU market under regulation 655/2013.
News
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.
Obelis officially welcomes NEW Proposals of European Medical Device Legislation
EU regulatory and compliance experts Obelis welcome proposal of new medical and in-vitro diagnostic device legislation for Europe.
TTIP and SMEs: what potential?
Learn more about the potential benefits the Transatlantic Trade and Investment Partnership may have for small-to-medium-sized enterprizes across the EU and US.
Public workshop by EC on NEW medical device regulations
The EC's public workshop on the proposed new EU medical device regulations held in February 2013 included talks on scope, requirements, and compliance.
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.
Obelis Featured on Important Suppliers Directory
The Obelis Responsible Person Center (O.E.R.P.C) has been featured on personalcaresuppliers.com, a leading portal for USA personal care product suppliers.
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.