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.
New regulations in France aim to strengthen accident prevention and management for ICPE/Seveso sites. Compliance deadlines extend to 2026 for new installations. Regular monitoring and reporting are key to meeting regulatory obligations. SAFE Factory software to automate ICPE/Seveso status tracking and ensure compliance with the latest regulations.
The European Commission's CSS Roundtable members developed 10 recommendations for the SSbD concept to advance science, trade, and sustainability in the EU. The SSbD framework aims to promote safer and more sustainable chemicals by design, stimulate innovation, and comply with EU regulations.
On March 25, the European Commission adopted clarifications regarding the update of the information requirements under the REACH regulation. 23 changes have been officially added to the annexes of the European regulation.
The IFRA 49 deadline is approaching on May 10, 2022. Compliance with IFRA standards is crucial for fragrance safety in cosmetic products. Learn how to ensure compliance and avoid issues with fragrance suppliers. Finished products on the market do not need to be withdrawn, but modifications may be necessary.
The digital transformation of the cosmetics industry is reshaping marketing, manufacturing, and customer experiences. As environmental concerns grow, regulations are evolving, impacting packaging and ingredient use. Meanwhile, China and India present new regulatory challenges and opportunities.
Explore the complexities of CBD in food supplements, classified as Novel Foods in the EU. Despite growing market interest, no CBD forms are approved for supplements yet. Legalization efforts continue, with regulatory challenges and varying national laws shaping the landscape.
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