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 risks of non-compliance with the new medical devices regulation in Europe, including financial losses, damage to brand image, and sanctions by Member States. Understand evolving obligations and how to ensure compliance to avoid these risks.
The new Medical Device Regulation expands the scope to cover non-medical devices and changes device classifications. Notified Bodies are now under stricter control, leading to longer time to market. Economic operators have specific roles and obligations. Stricter rules for clinical evaluation and post-marketing monitoring. A unique identification system and EUDAMED database enhance traceability. Regulation 2017/745 aims to improve transparency and safety of medical devices in Europe.
The European Commission released an addendum clarifying banned claims in cosmetics for hand gels. The document provides a negative list of prohibited claims and images. Understanding the difference between cosmetic and biocidal products is crucial for marketing strategies. Consider the advantages of marketing a leave-on cleansing gel versus a hand disinfectant.
The European Commission's REACH Committee has approved the postponement of the authorisation deadlines for ethoxylated 4-(1,1,3,3-tetramethylbutyl)phenol, crucial for Covid-19 related medical products. The new deadlines extend the application and sunset dates by 18 and 36 months, respectively.
DGCCRF found 38% of hand sanitizers non-compliant, risking ineffectiveness against Covid-19. Learn how to ensure compliance with biocidal regulations to avoid product recalls.
Learn about UFIs, unique codes required on labels of hazardous mixtures. Deadlines for compliance are set for 2021 and 2024. Harmonised format for poison centre notifications is now mandatory in the EU.
