RegAffairs AI

RegAffairs AI gives Claude cited answers to regulatory and compliance questions, drawn from more than 1,400 datasets published by regulators in 49 jurisdictions, including the EU, UK, US, Canada, Brazil, Mexico, India, Turkey, Japan and Australia. Sources include ECHA, EFSA, the European Commission, FDA, EPA, EMA, HSE, Health Canada, ANVISA, CDSCO and FSSAI.

Ask what a regulation requires, whether a substance or ingredient is allowed, what a limit is, what a registration needs, or what changed, and every claim links to the official document it came from.

What it covers:

• Chemicals: REACH (SVHC Candidate List, Annex XIV and XVII), CLP harmonised classification, UK REACH, US TSCA, California Prop 65, Turkey KKDIK.
• Food: EU and US additives, novel foods, food contact, contaminants, labelling, allergen and health claim rules.
• Pharma: EU GMP (EudraLex Volume 4), 21 CFR 210/211, ICH guidelines, EMA, FDA and Health Canada drug data.
• Medical devices: EU MDR and IVDR, FDA classification and PMA, notified bodies, CDSCO device lists.
• Cosmetics: EU Regulation 1223/2009 Annexes II to VI, plus UK, US, Canadian and ASEAN ingredient lists.
• Pesticides: EU approvals and MRLs, US EPA tolerances, Brazil ANVISA data.
• Biocides: EU BPR active substances, the Article 95 list, EPA disinfectant lists.
• Workplace safety: exposure limits from HSE EH40, TRGS 900, INRS, INSST and OSHA.
• Textiles: ZDHC MRSL, OEKO-TEX Standard 100, labelling rules.

Every result carries the source's title, date and a link to the stored document. When the data holds no record, the answer says so and names what was searched.

Built for regulatory affairs, compliance, product stewardship, SDS authoring and consultancies. Lookup tools are read-only; a full question is saved to your RegAffairs AI history and counts on your plan. RegAffairs AI uses public regulatory data and is not affiliated with any regulator. Answers are research, not legal advice.