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
Discover how a dedicated cosmetic PLM software centralizes your data, ensures compliance, and speeds up product time-to-market.
Recevez une fois par mois les dernières actus réglementaires et conseils d’experts.
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.
Learn about the exclusion and substitution criteria for active substances in biocidal products under the Biocidal Products Regulation. Discover how stakeholders can contribute to the decision-making process and the importance of public consultations.
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