Modular Solution for Cosmetics Compliance
Checking the Conformity of your Formulas
Compliance of your Regulatory Files
Flexible Software Solution for Product Compliance
Regulatory Monitoring Tool
Platform for the Traceability of Risky Substances
Software for Creating and Managing SDS
Software for managing your chemical risk
Worldwide Compliance for your Cosmetics, Fragrances & Skincare Products
U.S. cosmetics compliance
Compliance of your Food Supplements
Regulatory Services for Chemicals in Europe
Support for Authorization Files
Register your Chemical Substances in Europe
Customized Regulatory Monitoring of your Substances
Biocides Product Compliance
Marketing Authorization for Biocides
Collaborative Approach to Biocides Marketing Authorization
Regulatory Monitoring of Biocides
Support for your Safety Data Sheets
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.
Explore the EU Detergent Regulation revision-new product passports, digital labeling & stricter safety standards—all promoting a sustainable, toxic-free market.
Ensure your biocidal products comply with EU regulations. Learn about labeling, advertising, and claim requirements to avoid penalties and ensure safety.
Discover the upcoming approval of Trihydrogen pentapotassium di(peroxomonosulfate) di(sulfate) for biocides. Learn how EcoMundo can assist with compliance.
Join EcoMundo's consortium for Formic Acid regulation. Benefit from cost sharing, economies of scale, and streamlined authorization. Deadline: Oct 31, 2024.
Join EcoMundo's consortium for Chrysanthemum PT18 regulation. Benefit from cost sharing, economies of scale, and streamlined product authorization.
Join EcoMundo's consortium for ADBAC/BKC PT2 regulation. Benefit from cost sharing, economies of scale, and streamlined product authorization. Deadline: June 30, 2025.