Modular Solution for Cosmetics Compliance
Checking the Conformity of your Formulas
Compliance of your Regulatory Files
Flexible Software Solution for Product Compliance
Regulatory Monitoring Tool
Platform for the Traceability of Risky Substances
Software for Creating and Managing SDS
Software for managing your chemical risk
Worldwide Compliance for your Cosmetics, Fragrances & Skincare Products
U.S. cosmetics compliance
Compliance of your Food Supplements
Regulatory Services for Chemicals in Europe
Support for Authorization Files
Register your Chemical Substances in Europe
Customized Regulatory Monitoring of your Substances
Biocides Product Compliance
Marketing Authorization for Biocides
Collaborative Approach to Biocides Marketing Authorization
Regulatory Monitoring of Biocides
Support for your Safety Data Sheets
Les récentes conclusions de l'ECHA mettent en lumière des manquements aux normes REACH et POP dans la conformité de cosmétiques, pointant du doigt deux familles de substances chimiques à haut risque, les siloxanes cycliques et les composés perfluorés, en pointant du doigt des substances chimiques à haut risque comme les siloxanes cycliques et les composés perfluorés. Pour l'industrie cosmétique, se tenir informé des évolutions réglementaires est essentiel pour garantir la sécurité, la durabilité des produits, et la confiance des consommateurs.
Recevez une fois par mois les dernières actus réglementaires et conseils d’experts.
Learn about the approval of ADBAC/BKC and DDAC for disinfectants and the importance of preparing MA dossiers before the approval date. Join a biocide consortium to reduce costs and optimize your regulatory work. Register for our webinar on 10th November for more information.
From 1st January 2021, companies must notify hazardous mixtures in a new harmonised format. This blog explains the requirements and deadlines for compliance with the CLP Regulation. Learn about generating UFIs and why harmonisation is important for poison control centres.
The AGEC law, effective in France since 2021, aims to reduce waste and improve consumer information, impacting industries like cosmetics. Key measures include phasing out single-use plastics by 2040 and requiring detailed packaging labels, sparking manufacturer concerns.
Color additives are the only cosmetic ingredients in the United States that require pre-market FDA approval. This article shows you the main points to consider when launching a cosmetic product that contains color additives.
Despite significant costs to businesses, REACH authorisation offers substantial benefits, including improved health and environmental protection, reduced use of hazardous substances, and promotion of innovation. The societal benefits far outweigh the health risks.
Disinfectants can be classified as either medical devices or biocides based on their use. Medical device disinfectants are used for non-sterilizable reusable devices and must comply with EU Regulation 2017/745, while biocides follow EU Regulation 528/2012. Understanding the correct classification is crucial for compliance.
