Revision of SCCS Guidance on the Safety of Cosmetics – What has Changed?
News

Notes of guidance: The latest edition of the “Notes of guidance for testing of Cosmetic Ingredients and their Safety Assessment” has been issued and closed for comments following the deadline o [...]

Fragrance Industry – The End of Animal Testing in Allergen Risk Assessment
News

On the 16th of December lasy year, during the third annual review of the IDEA Project regarding risk assessment methodologies processes and criteria to identify fragrance allergens of concern, the Fra [...]

NEW SCCS opinion on o-Phenylphenol
Industry News, News

On December 15th, 2015, the Scientific Committee on Consumer Safety (SCCS) revised its opinion from June 25th on o-Phenylphenol, concluding that lowering the maximum concentration limit for this subst [...]

EC identified essential principles in REACH data-sharing
Industry News, News

On the 26th of January 2016 the new Regulation (EU) No 2016/9 entered into force. It defines extensively the terms of transparency, fairness and non-discrimination of data-sharing agreements for the r [...]

CoRAP 2016-2018 Published
News

On October 28th, 2015, the European Chemical Agency (ECHA) has published its proposal to update the Community Rolling Action Plan (CoRAP) for 2016-2018. The final plan will be adopted in March next ye [...]

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Obelis European Responsible Person Center (O.E.R.P.C.)

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.

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