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Service Provider - Cosmetics regulation 1223 2009

3 Companies

1 Product

MAZURKA SARL

Luxembourg

MAZURKA specializes in the application of cosmetic product regulations for companies with branded cosmetics. It assists them launch and follow up cosmetic products in the European market to comply with EC regulation 1223/2009. The DIP required before marketing includes many elements defined by European legislation. It also offers assistance during inspection authority missions. Fully conversant with trace one software.

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INVITRO-CONNECT GMBH

Switzerland

INVITRO-CONNECT GmbH – your international experts for laboratory tests and regulatory services. More than 80 testing laboratories and over 20 years of experience in the sector. We offer regulatory expertise and complete laboratory services for legal regulations such as: REACH regulation (EG) No. 1907/2006), biocide regulation (EG) No. 528/2012, GHS/CLP regulation (EG) No. 1272/2008 (CLP-VO), cosmetics regulation (EG) No. 1223/2009, medical device regulation (EU) 2017/745 (Medical Device Regulation – MDR) / ISO 10993, medical products for animals regulation (Directive 2001/82/EG -> (EU) 2019/6), medical foodstuffs for animals regulation (Directive 90/167/EWG -> (EU) 2019/4), Pesticides and plant protective products regulation (EU) 1107/2009, pharmaceutical regulation: Monitoring of all preclinical studies. We would love to be your reliable partner for all your laboratory testing and regulatory project needs. Dr. Ute Hassmann, Deputy Managing Director and Mr. Pascal Piller, Managing Director.

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TAOBÉ CONSULTING

Belgium

If you want to sell your cosmetics in Europe and the United Kingdom it is vital that they comply with EU regulation (CE) 1223/2009, which applies in 31 EU countries and the UK. This is widely considered to be the strictest regulation in the world. There are numerous criteria to consider when assessing the compliance of cosmetic products for Europe, which requires a safety assessor to examine all the documentation covering the ingredients used in the product's composition. The safety assessor also studies relevant toxicological data in order to establish a cosmetic product safety report (CPSR). Only at the end of this assessment can the product information file be completed and the product labels reviewed to ensure they include all the requisite information. The final phase of every registration project is to submit the notification to the appropriate portal (CPNP and/or SCPN). Taobé Consulting is cosmetic regulatory service provider with offices in Brussels (EU) and London (UK). We are experts at the registration of cosmetics in Europe and Great Britain. We create the CPSR, product Information File (PIF), check the formula, labels and claims for compliance. Taobé Consulting can also act as your EU and UK Responsible Person and notify your products on the CPNP and SCPN. In need of a regulatory service for another market? We’ll introduce you to one of our partners from our global network. Let’s talk! We are fluent in English, French, German, Spanish, Portuguese and Japanese.

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Certification etoxisafe®

COSMETIC PRODUCT SAFETY REPORT (CPSR) AND PIF CREATION

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Service Provider - Cosmetics regulation 1223 2009

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3 Companies