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 European Commission proposes to extend the obligations of the PIC Regulation by adding new substances subject to notification or prohibited from export starting October 2026.
Recevez une fois par mois les dernières actus réglementaires et conseils d’experts.
Explore the accelerated and simplified processes for placing disinfectants and sanitizers on the market during the Covid-19 pandemic. Learn about exemptions, compliance requirements, and the role of active substances in ensuring these essential products meet regulatory standards.
ECHA is speeding up the commercialisation of disinfectants and sanitizers during Covid-19. National derogations are being granted to procure active substances, like France's directive allowing temporary use of new sources. ECHA is also accelerating the process of inclusion to the approved suppliers list of Article 95. Learn more about biocidal products and Article 95.
Learn the differences between cosmetic and biocidal products, and the regulations that apply to each. Discover how to commercialize your leave-on cleaners effectively in the current market context. Explore the increasing demand for sanitizing products and how to meet it.
In collaboration with the Ministry of Ecological and Solidarity Transition, EcoMundo provides you with the Ministry's Frequently Asked Questions dedicated to hydroalcoholic gels.
California companies selling cleaning products must disclose ingredients on designated lists by Jan 2021. Act applies to air care, automotive, cleaning, and polish products. Background and compliance guidance provided.
The European Commission has postponed the implementation deadline for the medical devices regulation to May 26, 2021, due to the increased demand caused by Covid-19. This regulation harmonizes the legislation for medical devices in Europe, ensuring consumer safety.
