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.
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.
Discover the simplified authorisation process for eco-friendly biocidal products. Learn about eligibility, application, and fees to streamline your approval.