Modular Solution for Cosmetics Compliance
Check the Conformity of your Formulas
Secure your regulatory documents for each zone
Optimize on-site risk management
Manage your Safety Data Sheets efficiently
Automate your regulatory monitoring
Ensure the traceability of your substances
Maintain good HSE risk management
Are you planning to place a biocidal product on the European market through a simplified authorisation (simplified BPR authorisation), but find the regulatory requirements, expected data, and national specificities complex?
Recevez une fois par mois les dernières actus réglementaires et conseils d’experts.
Following the entry into force of Annex VIII of the CLP Regulation, Member States have started to adapt their systems for notification to the poison centre on the ECHA portal or have kept, to some extent, their own national systems in parallel.
.webp)
