New EC guidelines detail relevant data to be considered as minimum when detailing a Product Information File for cosmetic products on the EU market.
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.
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.
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.
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.
Stricter labelling principles for sunscreens in Europe
A new EU Commission recommendation, in line with 2006/647/EC) mandates the standardization of claims and labelling for sunscreen products on the EU market.
Obelis presenting at US Commercial Services Webinar
Obelis COO Doram Elkayam will join the 2013 US Commercial Services webinar to talk about EU cosmetic regulations and compliance obligations.
Safe Cosmetics Act of 2011 in the USA
Learn about the 2011 Safe Cosmetics Act and what implications it may have for the registration, labelling, and compliance of your products on the US market.
Animal by-products EU regulation on Medical and Cosmetic products
Find out the definition of an animal by-product and what EU legislative guidelines apply to medical and cosmetic products containing them within the EU market.
EUCORE Workshop: The New European Regulation on Cosmetics
Obelis and Israeli Chamber of Commerce organise EUCORE event for cosmetics manufacturers looking to introduce products to the EU market.