A regulatory affairs consultant's first answer, in seconds

Ask the question you'd send a regulatory affairs consultant and get a cited answer in seconds, straight from official regulatory text.

Self-serve and free to try.

Try it free. No credit card, no enquiry form and no call.

Skip the enquiry for your next regulatory affairs consulting lookup. Ask for the list entry, annex, amendment or deadline. The cited answer and research trail come together, and you can open the original text to check it.

What you'd ask a regulatory affairs consultant, answered today

Type a substance, a product or a market.

• Status checks: is it listed, restricted or authorised, and what changed after the last amendment or ruling?
• Comparisons: one product across several territories, keeping only the differences that matter. Those are thresholds, triggers, language duties and who holds the registration. Ask whether salicylic acid is allowed in leave-on cosmetics in the EU and the UK, and at what maximum concentration.
• Duty holders: who notifies, by when and under which article. "Which substances were added to the REACH SVHC Candidate List in the latest update, and what do article 33 and SCIP require of an article supplier?" comes back cited to the article.

Our guide to the SCIP database follows the same trail at article length.

RegAffairs AI vs regulatory affairs consulting, side by side

Ask a quick question for an answer in seconds, or use deep research for a longer run. Every claim links to the stored source document, with the research trail on the page.

Every answer cited to the official source

Type the question in plain language. The agent searches official registers, including the ECHA Candidate List, REACH Annex XIV and XVII, the C&L inventory, CosIng, the EU food additives and pesticides databases, TSCA, UK REACH, KKDIK, FDA and EMA registers. Inline citations open the stored source at the annex entry or judgment paragraph.

The research trail shows every search the agent ran and every document it read.

The homepage example asks: "Is TiO2 still harmonised as Carc. 2 under CLP?" It shows six research steps in 48 seconds, with sources from EUR-Lex and CURIA.

You can check every line, and so can the manager, lawyer or customer you forward it to.

Make regulatory affairs consulting hours count

Already work with a consulting firm? Run the research here first. Arrive with the cited facts, the market-by-market differences and the open questions already scoped. The brief gets shorter. The hours you pay for go on the decision, not on a search of EUR-Lex.

One question across markets and industries

Search chemicals, pharma, medical devices, food, pesticides, cosmetics and biocides through one question. RegAffairs AI joins official sources across markets, so you compare requirements without separate searches.

"Is DEHP (CAS 117-81-7) restricted under REACH Annex XVII, UK REACH and US TSCA, and how do the restrictions differ?" comes back as one cited answer. Ask in your own language and the answer comes back in it. New sources are added every week. The full list is on the coverage page.

Regulatory affairs consulting costs and published AI pricing

The Free plan needs no credit card. It searches the full corpus across every jurisdiction, research trail included. Pro is $100 per user per month: unlimited questions, deep research and priority speed. Month to month, no contract and no cancellation fee. Enterprise is available on request for seats, SSO and procurement.

Regulatory affairs consulting services are quoted per engagement. Here you can ask a real question before you pay anything, and budget the month without a sales call. See pricing.

Who asks here before calling a regulatory affairs consultant

• In-house regulatory affairs and product stewardship at chemical, coatings and ink makers: SVHC, Annex XVII or CLH checks.
• Pharma and medical device RA teams: EMA, FDA and national registers. Our GMP Canada guide covers what a foreign site needs to show for a Health Canada establishment licence.
• Cosmetics and food teams: CosIng, SCCS opinions, additives, contaminants and health claims.
• Pesticides teams: EU PPP entries and MRLs in the same pass.
• Only Representatives: KKDIK registration requirements and deadlines across client portfolios.
• SDS authors: classifications, exposure limits and the lists that belong in section 15.
• Founders entering a new market: its rules, before they contact regulatory affairs consulting companies.

FAQ

Can RegAffairs AI replace a regulatory affairs consultant for routine questions?

Status, scope, multi-market and deadline questions get a cited answer from the regulator's own text. You can finish that lookup without opening an engagement.

How much does regulatory affairs consulting cost compared with RegAffairs AI?

Regulatory affairs consulting firms quote per engagement, and their service pages don't list rates. RegAffairs AI is free to try, and Pro adds unlimited questions and deep research.

Are my questions kept confidential?

Questions are never used to train models. Data is processed and stored in the EU by default.

Ask it before you send the enquiry

Ask the question you were going to send to a consultant. Get the answer, open the citations and put the research to work.

Try it free or see pricing.