Modular Solution for Cosmetics Compliance
Check the Conformity of your Formulas
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Manage your Safety Data Sheets efficiently
Automate your regulatory monitoring
Ensure the traceability of your substances
Maintain good HSE risk management
Learn how to navigate UK REACH requirements with a step-by-step guide on submitting a Downstream User Import Notification (DUIN) by the deadline. Understand the necessary information for different import volumes and subsequent registration obligations to ensure compliance.
Recevez une fois par mois les dernières actus réglementaires et conseils d’experts.
Biocidal Products Regulation (BPR) EU No. 528/2012, which replaced the Biocidal Products Directive. It highlights the European Commission's extension of approval for two substances and the loss of approval for ten others, detailing the implications for the market.
ECHA recommends adding 8 SVHC to the REACH authorization list to eventually ban their use in Europe. Lead is a key substance under consideration. Learn more about the process and implications of this recommendation.
New hazard classes for CLP regulation of substances and mixtures enter into force on 20 April 2023. Learn about the new classifications for endocrine disruptors, PBT, vPvB, PMT, and vPvM substances, and the transition period for compliance.
Learn about photoinitiators in dietary supplements, their safety issues, regulations, and guidelines for safe use. Discover how to reduce health risks associated with photoinitiators in dietary supplements.
Learn about food additives, their functions, and regulations in the EU. Discover key references like Regulation 1333/2008 and 231/2012. Explore the authorization of new additives like carbomer and glycosylated steviol glycosides in food supplements. Understand the importance of compliance with EU regulations for food safety.
ECHA is harmonizing its platforms to streamline data submission for REACH, CLP, and more. New obligations and resubmissions are on the horizon. Learn about the usefulness of ECHA's platforms and where to get help with regulatory dossier submissions.