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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.
Learn about the key labelling requirements for Over-the-Counter (OTC) products in the US. From general drug labelling to OTC-specific requirements and OTC monograph labelling, ensure compliance to avoid FDA regulatory action.
Starting January 2021, suppliers of articles containing SVHCs must submit information to the SCIP database. Manufacturers, importers, and distributors in the EU are affected. SCIP aims to provide access to information on SVHCs in articles.
The Scan4Chem app by LIFE AskREACH helps consumers check for harmful substances in products. Companies can benefit by ensuring traceability of SVHCs. Learn more about SVHCs and AskREACH.
Learn about the upcoming changes in medical device regulations. By May 2021, all devices must comply with the new EU Regulation. Find out the deadlines for re-certification and how this impacts medical devices on the market.
Explore recent regulatory changes in the EU, including microplastic restrictions, microbial safety guidelines for packaging, and updates to IFRA standards. Discover international shifts in cosmetic regulations in Russia, Saudi Arabia, and China, and insights from the Chartres Congress.
New REACH provisions require registrants to update dossiers by 1st January 2020. Changes include nanoform characterisation and safety assessment. Industry finds deadline too tight. Learn more about registering nanoforms and REACH annex changes.