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.
Discover how ECHA accelerates the approval of disinfectants and sanitizers during COVID-19 by streamlining processes and granting temporary exemptions.
In collaboration with the Ministry of Ecological and Solidarity Transition, EcoMundo provides you with the Ministry's Frequently Asked Questions dedicated to hydroalcoholic gels.
Discover Canada's expedited licensing measures for hand sanitizers during COVID-19, ensuring availability while meeting Health Canada's interim guidelines.
Discover how the French government facilitated hand sanitizer commercialization during COVID-19 with regulatory exemptions and compliance guidelines.
Learn how Brexit affects UK biocidal product authorizations and steps companies need to take to comply with EU regulations. Expert guidance available.
Learn about the "same" biocidal product Marketing Authorisation (MA) process, dossier submission, evaluation, and fees for EU regulations.
