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
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.
Recevez une fois par mois les dernières actus réglementaires et conseils d’experts.
Navigate the new Medical Device Regulation with ease. Discover changes in classification, roles, and compliance to ensure safety and transparency in Europe.
Discover the key changes in the EU Medical Devices Regulation, its impact on classifications, compliance deadlines, and implications for businesses.
Ensure your medical devices comply with Regulation (EU) 2017/745. Learn about certification deadlines and requirements for new and existing devices.
