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
The active substance prallethrin has been approved for PT18, with an effective date of March 1, 2026. This new regulation requires market players to urgently prepare a market authorization (MA) dossier to continue selling their products, under penalty of withdrawal from the market.
Recevez une fois par mois les dernières actus réglementaires et conseils d’experts.
Learn about the national marketing authorisation process in France, mutual recognition, dossier submission, and fees. Find key resources and guidelines.
Discover the Union MA process for biocidal products, enabling EU-wide market access without national authorisation. Learn about dossier submission and fees.
Discover the ins and outs of biocidal marketing authorisation types, applications, and timelines at national and European levels. Expert advice available.
Explore the BPC's work programme and recent opinions on active substances like Margosa extract and Fludioxonil. Learn more on ECHA's website.
Discover why the FDA banned 19 ingredients in antibacterial soaps, including triclosan, and learn about the potential risks and alternatives.
Discover the essential steps of biocidal risk assessment: hazards, exposure, and risk characterization. Get expert guidance on biocidal product regulations.
