Cosmetic Regulatory Compliance

AI specialist for cosmetic adverse event reporting under EU Regulation 1223/2009 and MoCRA. Classify serious undesirable effects, draft competent authority notifications, and manage post-market surveillance.

AI expert for substantiating cosmetic claims under EU Regulation 655/2013 and FDA guidelines. Build evidence dossiers, review claim language, and avoid borderline drug claims.

AI assistant for cosmetic ingredient safety assessment. Evaluate toxicological profiles, NOAEL values, and exposure margins to meet EU, FDA, and global cosmetic regulations.

AI advisor for cosmetic label compliance across EU, FDA, and global markets. Draft and review INCI lists, claims, warnings, and mandatory label elements to avoid regulatory rejections.

AI advisor for cosmetic stability testing protocols, shelf-life determination, and PAO compliance. Design accelerated stability studies and interpret results for regulatory documentation.

AI advisor for cosmetic market entry regulatory strategy across EU, US, China, and ASEAN. Plan registration timelines, documentation requirements, and compliance roadmaps for new markets.

AI assistant for drafting EU Cosmetic Product Safety Reports (CPSR). Structure Part A and Part B, compile toxicological data, and prepare documentation ready for safety assessor review.

Expert AI assistant for EU Cosmetics Regulation (EC) No 1223/2009 compliance. Navigate Annex listings, CPNP notifications, labeling rules, and responsible person obligations with ease.

AI assistant for verifying INCI names, ingredient ordering, and cosmetic formula compliance. Detect naming errors, validate Annex status, and prepare compliant ingredient declarations.

AI advisor for cosmetic preservative systems, PET testing, and microbiological compliance. Evaluate preservative efficacy, select compliant alternatives, and interpret ISO 11930 results.