Modular Solution for Cosmetics Compliance
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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.
The European Commission postponed the ban on DEHP in medical devices due to concerns about its adverse health effects. Learn about the regulation changes and deadlines for authorization to use DEHP in medical devices. Find out more about DEHP and its effects.
Food supplements are concentrated sources of nutrients or other substances with a nutritional effect. The industry is facing stricter regulations to ensure safety and efficacy. Regulatory obligations vary by country, with compliance being crucial for safety and accuracy.
Probiotics and prebiotics are essential for gut health. Learn about the differences between them, the official authorization of the term "probiotics" for food supplements, and the conditions that must be met to use this term on labels.
The European Commission has approved Chrysanthemum cinerariaefolium extract for use in type 18 biocidal products, effective February 1, 2025. This decision follows a thorough evaluation under Directive 98/8/EC, aiming to enhance pest control measures.
Formic acid has been approved as an active substance for TP 2, 3, 4, and 5 from November 1, 2024, to October 31, 2034. The authorization of biocidal products containing it requires risk assessments, user category considerations, and residue analysis to ensure safety.
The European Commission's 19th and 20th ATPs amend Annex VI of CLP, revising classifications for boron compounds and 2-EHA. New notes provide guidance on hazard additivity and classification. These changes impact the chemical industry, requiring compliance by February 2025.
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