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
Managing cosmetic regulatory data across the U.S., Canada, and Europe is no longer just a compliance issue. It is a data management challenge that directly impacts consistency, risk, and scalability for cosmetic brands.
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Learn about the upcoming public consultation on REACH authorisation for low volumes and legacy spare parts. Find out how to contribute and make your voice heard.
ECHA's new compliance strategy aims to improve efficiency and transparency in dossier evaluations, focusing on substances harmful to health and the environment. Registrants must update dossiers promptly to meet new deadlines and avoid unnecessary tests.
The European Commission has set up a set of indicators to measure the relationship between chemical substances and their impacts, as well as the role played by the regulations in place in their reduction. Unfortunately, the lack of available data hampers this operation.
ECHA's new compliance strategy enhances dossier evaluation efficiency and transparency, focusing on critical substances for health and the environment. Registrants have specific timelines to comment and update dossiers, with flexibility for certain testing proposals.
This blog provides a comprehensive guide on transitioning to the CLP regulation for chemical products, highlighting key compliance steps for manufacturers, importers, downstream users, and distributors. It covers classification, labeling, and Safety Data Sheets requirements, ensuring adherence to the 2015 deadline.
Companies importing or manufacturing substances from 1 to 100 tons a year must register by May 31, 2018. Learn about the process and deadlines for REACH 2018 compliance.