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.
Discover how Brexit impacts the biocides industry, including compliance changes and obligations for UK-based companies. Prepare for the transition now.
Discover the extended deadline for hydroalcoholic product compliance in France. Learn about the transition phase and labeling requirements until December 2020.
Discover the differences between biocidal and REACH Letters of Access (LoA) and learn how they impact compliance, marketing, and testing requirements.
Explore the US temporary guidance for hand sanitizer commercialization during COVID-19. Learn about formulation, requirements, and market entry strategies.
Discover how ECHA simplifies biocidal product regulations during Covid-19. Learn about exemptions, compliance, and market authorization for disinfectants.
Discover how ECHA accelerates the approval of disinfectants and sanitizers during COVID-19 by streamlining processes and granting temporary exemptions.
