RegAffairs AI

Answers a regulatory question that needs reasoning across several sources, jurisdictions or industries, or one that no industry tool covers. Examples: "is X restricted and what must my SDS say", "compare EU and GB rules for Y", "who must notify, by when, under which article". The tool runs the RegAffairs AI research agent over more than 1,400 regulator datasets and returns a written answer with nu

Fetches the result of a `regaffairs_ask_question` call that returned `status: "running"` and an `answer_id`. It waits up to 40 seconds and returns the finished answer with citations, or `running` again. It does not count as a new question. Not intended for starting a new question.

Searches the wording of regulations, guidelines and register entries, for questions that need the text rather than a written answer or that fall in an area no industry tool covers, such as REACH or CLP article text, drinking water limits or industrial emissions reporting. It runs a ranked full-text search over every live dataset and returns passages with citations. It does not count as a question.

Lists what RegAffairs AI covers ("do you have the EU Cosmetics Regulation?", "which Brazil pesticide registers are in?", "what do you cover for food in the UK?"), and checks before answering that a regulation or register is available. It returns the live catalogue: dataset id, plain name, regulator, jurisdiction, industry, what it contains and when it was last refreshed. Filter by industry, jurisd

Checks whether one or more chemical substances (name, CAS or EC number) are registered, listed, restricted or banned, and screens a bill of materials. It resolves the identity against the ECHA C&L Inventory and REACH registered substances, the EU customs inventory (ECICS), the US TSCA Inventory, the Australian AICIS inventory and the Turkish chemical inventory. It then checks the ECHA SVHC Candida

Looks up a substance's hazard classification, GHS pictograms, H-statements, signal word or label elements (for example for SDS sections 2 and 3 or a CLP label), and its UN number and transport hazard class (SDS section 14). It returns the EU CLP Annex VI harmonised entry (hazard classes and categories, H-statements, pictograms, signal word, specific concentration limits, M-factors and the ATP that

Looks up occupational exposure limits for a substance (OEL, WEL, PEL, AGW, VLEP, MAC, STEL) in one or more countries, for example for SDS section 8, a COSHH assessment or an OSHA compliance check. It covers HSE EH40 and the COSHH Regulations 2002 (GB), TRGS 900 and the GESTIS substance database (Germany), INRS VLEP tables (France), INSST LEP (Spain), the SER database (Netherlands), FOD WASO limits

Checks whether a food additive (E-number), colour additive, novel food, vitamin or mineral form, food contact substance or contaminant limit is allowed, and under which conditions, in the EU or US. EU coverage: Regulation (EC) No 1333/2008 Annex II with food categories and maximum levels, the Novel Food Union list (Regulation 2015/2283), contaminant maximum levels (Regulation 2023/915), the food s

Answers what a food label must show (mandatory particulars, nutrition declaration, ingredients list, allergen emphasis, gluten-free, date marking), which allergens must be declared, and whether a nutrition or health claim is authorised. It covers the EU Food Information to Consumers Regulation (EU) No 1169/2011, the EU nutrition and health claims Regulation (EC) No 1924/2006 and its register, the

Checks whether a cosmetic ingredient is banned, restricted or permitted, and gives its INCI name, maximum concentration, product-type conditions and label warnings. It covers the EU Cosmetics Regulation (EC) No 1223/2009 Annexes II to VI with entry numbers, the EU common ingredient names glossary (Decision 2019/701, the last published edition), the UK cosmetics rules and UK ingredient opinions, th

Checks whether a plant protection active substance is approved, banned or under review, and gives the maximum residue level (MRL) or tolerance for a crop. EU coverage: approvals under Regulation (EC) No 1107/2009, candidates for substitution, emergency authorisations, MRLs under Regulation (EC) No 396/2005, and the EU fertilising products Regulation 2019/1009 for biostimulants. GB: the HSE active

Checks whether a biocidal active substance is approved and for which product types (PT1 to PT22), whether a supplier is on the Article 95 list, whether a biocidal product or disinfectant is authorised, and which EPA-registered disinfectants work against a pathogen. EU coverage: BPR active substance approvals, the Article 95 supplier list, Union authorised biocidal products, BPC opinions and the pr

Finds what a GMP or ICH guideline requires and the text of a GMP annex or ICH guideline, and checks whether a UK site holds an MHRA manufacturing or wholesale (GMP/GDP) licence. It covers EU GMP (EudraLex Volume 4, Parts I to IV and Annexes 1 to 21), US cGMP for finished pharmaceuticals (21 CFR Parts 210 and 211), the ICH Quality, Safety, Efficacy and Multidisciplinary guidelines and the ICH M4 Co

Checks whether a medicine is authorised in a market, with its approval details and shortage status, or a medical device's classification, registration, approval or notified body. Medicines: the FDA Orange Book (approved drugs, therapeutic equivalence, patents and exclusivity), EMA authorised medicines, EMA orphan designations, the EMA, FDA and MHRA shortage lists, the Health Canada Drug Product Da

Checks whether a substance is restricted in textiles, clothing, footwear or leather and what limit applies under a brand or certification list, and what a textile fibre, care or flammability label must show. Substance lists: the ZDHC MRSL, OEKO-TEX Standard 100 limit values by product class, the bluesign system substances list, REACH Annex XVII entries that apply to textiles and leather (for examp