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
Learn the key differences between US and EU cosmetic regulations and how to export your products from the USA to Europe in full compliance.
Recevez une fois par mois les dernières actus réglementaires et conseils d’experts.
Explore the EU's definition of cosmetic products under regulation 1223/2009, which outlines criteria for classification, including intended use and contact with specific body parts. Understand the nuances of borderline products and related regulations affecting cosmetics compliance.
Learn about the essential tools for REACH registration: IUCLID, Chesar, and REACH-IT. Discover the main changes coming in June 2016, including the mandatory switch to IUCLID 6 and REACH-IT 3. Strengthened user support and facilitated data exchange will help companies comply with the May 31, 2018 deadline.
Learn about the role of a Responsible Person (RP) in the EU cosmetic market. Discover who can be an RP, their obligations, and the importance of compliance with regulations and a solution to finding an RP.
Explore the unique methodology of biocidal risk assessment, which involves hazard identification, exposure assessment, and risk characterization. Learn about the specific tools and guidance used to evaluate risks to human health and the environment in this comprehensive process.
Cosmetic claims are marketing tools that describe a product's effects, help consumers choose, and make products more appealing. EU regulations ensure claims are truthful, supported by evidence, and enable informed decisions without misleading or denigrating competitors.
REACH registration ensures that companies provide data on the properties and risks of chemicals they manufacture or import into the EU. Non-EU companies can comply by appointing an Only Representative. The process is mandatory for substances over 1 tonne per year.
