On the 30th of November 2009, the new European Cosmetic Regulation, EC 1223/2009, was published in the official journal of the European Commission, hence putting it into force. The EC 1223/2009 …
To ascertain a better functioning of the European cosmetic market and a higher level of user protection, the New Regulation establishes a set of rules to be fulfilled by every cosmetic …
- “Only cosmetic products for which a legal or natural person is designated within the community as ‘responsible person’ shall be placed on the market” (Art.4, p.4). As clearly indicated …
Cosmetic EC 1223/2009 Services »The new Cosmetics Regulation EC 1223/2009 clarifies requirements for safety of a cosmetic product and includes clearer requirements for manufacturers to compile an encompassing Product Information File prior to placing a …
Prepared between 2002 and 2006 by ISO Technical Committee 217, Working Group 6, the ISO standard 22716:2007 was published in November 2007. While being an international standard, ISO 22716:2007 was adopted …
The Cosmetics Directive 76/768/EEC was published on July 27, 1976. It allows cosmetic products in the European Economic Area to circulate freely and ensures their safety for use. A cosmetic product …
In order to ensure that a cosmetic product complies with the Cosmetics Directive, the following steps must be taken:
Obelis International Offices (O.I.O.). A network aimed at creating local Obelis Offices around the world offering European Authorized Representative (EC REP) services to local markets ... read more
Obelis European Responsible Person Center (O.E.R.P.C.), is part of Obelis Group. Obelis s.a. established in Brussels, Belgium since 1988, provides European Authorized Representative (EC REP), EU Responsible Person & CE Marking advisory services to manufacturers worldwide (EU & Non-EU), all in accordance with European Directives & Regulations.
Our high quality compliance solutions, proven by our ISO 9001:2008 certification, include Classification, identification of EU standards, Technical Documentation review, Authorized Representative & EU Responsible Person, Product Notification & Product Registration to national EU Authorities, Labeling Compliance, GMDN Code Verification, Free Sales Certificates, Trade Mark submissions and many more.
While still retaining a unique expertise on cosmetics, medical devices & in-vitro diagnosis medical devices, Our team of experts will assist you in introducing or maintaining your product(s) circulation within the EU Market and guide you through the regulatory maze of product safety and requirements also for machinery, personal protective equipment, pressure equipment, radio and telecommunication equipment, electrical equipment, low voltage equipments, toys and other consumer goods.
Contact us today and let us help you meet your requirements.
Obelis is excited to announce the latest OneLink OneSolution advancement. While still retaining the core group of international compliance experts ... read more