Modular Solution for Cosmetics Compliance
Check the Conformity of your Formulas
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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.
Food supplements are concentrated sources of nutrients or other substances with a nutritional effect. The industry is facing stricter regulations to ensure safety and efficacy. Regulatory obligations vary by country, with compliance being crucial for safety and accuracy.
Formic acid has been approved as an active substance for TP 2, 3, 4, and 5 from November 1, 2024, to October 31, 2034. The authorization of biocidal products containing it requires risk assessments, user category considerations, and residue analysis to ensure safety.
The European Commission has approved Chrysanthemum cinerariaefolium extract for use in type 18 biocidal products, effective February 1, 2025. This decision follows a thorough evaluation under Directive 98/8/EC, aiming to enhance pest control measures.
The European Commission's 19th and 20th ATPs amend Annex VI of CLP, revising classifications for boron compounds and 2-EHA. New notes provide guidance on hazard additivity and classification. These changes impact the chemical industry, requiring compliance by February 2025.
The public consultation on the proposed restriction of 10,000 PFAS in the EEA concluded with over 6,000 comments, mainly from industry stakeholders seeking exemptions. ECHA will review these inputs, which highlight PFAS's critical role in various sectors despite environmental concerns.
Industry groups are challenging new EU labeling requirements, citing underestimated impacts on trade and product availability. Concerns include restrictions on environmental claims, increased label font size, and tight deadlines for updates, urging a reevaluation of the CLP Regulation.
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