EC Proposes to Restrict the use of Methylisothiazolinone (MI): Public Consultation now Open.

From the 29th of July 2015 to the 23rd of October 2015 public consultation on the restriction of the use of the preservative Methylisothiazolinone (MI) in cosmetics products is open. The EC proposes t [...]

10th Round of Negotiations – TTIP

The 10th round of negotiations for The Transatlantic Trade and Investment Partnership (TTIP) finished on July 17th 2015, in Brussels. In the course of the negotiations, the parties discussed all thre [...]

EC Restrict Hair Dye Ingredients after Adoption of New Regulation (EU) 2015/1190

On July 20, 2015 the European Commission adopted Regulation (EU) 2015/1190 thereby amending the Annex III to Regulation (EC) No 1223/2009. The new Regulation, binding in its entirety and directly appl [...]

SCCS to pronounce on the safety of four cosmetic ingredients

During the last week of June 2015, the Scientific Committee on Consumer’s Safety (SCCS) were requested to pronounce on the safety of four different cosmetics ingredients of potential concern, as us [...]

SCCS Opinion on “Silica, Hydrated Silica, and Silica Surface Modified with Alkyl Silylates (nano form)”

Silica, Hydrated Silica, and Silica Surface Modified with Alkyl Silylates (nano form) Silica, Hydrated Silica, Silica Silylate and Silica Dimethyl Silylate nano forms are used in many leave-on and [...]



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.

Contact us today and let us help you meet your requirements.