regaffairs_ask_question

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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 numbered citations. Sources include ECHA REACH and CLP lists, EU food, cosmetics, plant protection and biocides law, HSE, US EPA TSCA, FDA 21 CFR, California Prop 65, EudraLex Volume 4 GMP, ICH, EMA and Health Canada. Each citation links to the source document. The tool can take up to a minute. If it is still running, it returns `status: "running"` and an `answer_id` for `regaffairs_get_answer_status`. Each call counts as one question on the user's RegAffairs AI plan and is saved to their history. Not intended for a single fact that an industry tool answers (one substance's list status or classification, an exposure limit, an ingredient's status, an MRL, a drug or device register entry). Not intended for legal advice, clinical trial design or FDA submission strategy.