Modular Solution for Cosmetics Compliance
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Maintain good HSE risk management
Following the announcement by the MoEUCC, substances manufactured or imported into Turkey in quantities of at least one tonne per year must be subject to temporary or permanent registration with the KKS by 30 September 2026 at the latest.
Recevez une fois par mois les dernières actus réglementaires et conseils d’experts.
From 1st January 2021, companies must notify hazardous mixtures in a new harmonised format. This blog explains the requirements and deadlines for compliance with the CLP Regulation. Learn about generating UFIs and why harmonisation is important for poison control centres.
The AGEC law, effective in France since 2021, aims to reduce waste and improve consumer information, impacting industries like cosmetics. Key measures include phasing out single-use plastics by 2040 and requiring detailed packaging labels, sparking manufacturer concerns.
Color additives are the only cosmetic ingredients in the United States that require pre-market FDA approval. This article shows you the main points to consider when launching a cosmetic product that contains color additives.
Despite significant costs to businesses, REACH authorisation offers substantial benefits, including improved health and environmental protection, reduced use of hazardous substances, and promotion of innovation. The societal benefits far outweigh the health risks.
Disinfectants can be classified as either medical devices or biocides based on their use. Medical device disinfectants are used for non-sterilizable reusable devices and must comply with EU Regulation 2017/745, while biocides follow EU Regulation 528/2012. Understanding the correct classification is crucial for compliance.
Learn about the two new substances added to the Candidate List of Substances of Very High Concern and the implications for companies.