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
Active substance renewal under the GB Biocidal Products Regulation (GB BPR) is a critical regulatory challenge for companies placing biocidal products on the Great Britain market. With strict 550-day submission deadlines and major expiries in 2026 and 2027, early planning is essential to avoid market disruption and loss of product authorisations.
Recevez une fois par mois les dernières actus réglementaires et conseils d’experts.
Health Canada has updated cosmetic regulations to align with EU standards, requiring detailed ingredient disclosure, especially for fragrance allergens. Companies must notify Health Canada within 10 days of sale, ensuring labels include contact info and are bilingual.
The EU has reached a provisional agreement to ban the last uses of mercury in dental amalgams and certain lamps by 2025, aligning with its zero pollution goals. This move aims to protect health and the environment, supporting a transition to mercury-free alternatives.
The biocides industry is set for a major development with the approval of "Trihydrogen pentapotassium di(peroxomonosulfate) di(sulfate)" on July 1, 2025. This substance is approved for use in various biocidal products, including disinfectants and algicides, under specific conditions and labeling requirements.
Learn about the concerns surrounding microplastics in cosmetics, the EU's regulatory response, proposed restrictions, exemptions, and implementation timeline. Discover the reporting requirements and the EU's commitment to sustainable practices in the cosmetics industry.
Join a leading consortium for ADBAC/BKC PT2 regulation to benefit from cost sharing, economies of scale, and reduced compliance risks. With a dossier deadline of June 30, 2025, this collaboration offers financial savings and streamlined regulatory approval.
Join a consortium focused on Chrysanthemum PT18 regulation under the Biocidal Product Regulation. Benefit from cost sharing, economies of scale, and reduced redundancy in compliance efforts. Act before the dossier submission deadline on January 31st, 2025.
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