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The EU is reassessing its Cosmetic Regulation through a 2025 Fitness Check. Discover what this means for industry, safety, animal testing, and sustainability alignment.
Recevez une fois par mois les dernières actus réglementaires et conseils d’experts.
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.
Ozone, a powerful oxidant, is approved for use in biocidal products in categories 2, 4, 5, and 11, offering benefits like no toxic residue. Approval conditions include maintaining purity standards. Authorization is valid from July 2024 to June 2034.
Learn about CMR substances, their definitions, regulations, and classifications. Discover the main regulations, including CLP and REACH, that apply to CMRs to protect workers, consumers, and the environment. Explore where CMRs are located and the sectors affected by these hazardous substances.
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