Regulatory intelligence software that answers with the source
Ask a regulatory question and get a cited answer in seconds. RegAffairs AI is regulatory intelligence software that reads the official registers for you.
Every claim links to its source document, so you can check it before you share it. Free to try.
Try it free · See coverage. No credit card and no demo call.
Regulatory intelligence means knowing what regulators require of your substances, products and markets, and what is about to change. That knowledge is scattered. The SVHC candidate list, CLP Annex VI, the TSCA inventory, a Turkish KKDIK notice and an EU General Court judgment each sit in their own register, sometimes in their own language.
What regulatory intelligence software should do
It should answer the question you asked. A pile of search hits is just more homework.
- Plain questions. Ask in your own language. A substance name, a CAS number, a product or a market is enough.
- Cited answers. The agent checks status, scope, thresholds, deadlines and who holds the duty. Each claim cites the annex entry, article or judgment paragraph, and opens the stored document.
- Many markets at once. Check Germany, the UK and Turkey in one question.
- A visible trail. You see every search it ran and every document it read.
- Current sources. The corpus refreshes weekly, as a rule, and new sources are added every week.
- No setup. Start today, with no implementation project and no onboarding call.
A quick answer takes seconds. Deep research mode handles multi-step, multi-market questions.
Take the example on our homepage: "Is TiO2 still harmonised as Carc. 2 under CLP?" The answer cites Delegated Regulation (EU) 2020/217 and Judgment T-279/20 and T-288/20, paragraphs 105 to 112. It took 6 research steps and 48 seconds. The citation opens the paragraph, so the source can go straight into your report. More on why we cite the paragraph.
Regulatory intelligence across industries and markets
One question can cover the official registers of several industries.
| Industry | Official sources you can query |
|---|---|
| Pharma | EMA, FDA and national medicines regulators |
| Chemicals | ECHA REACH/CLP, SVHC candidate list, Annex XIV/XVII, TSCA, UK REACH, KKDIK |
| Food | EU food additives, contaminants, FIC, health claims |
| ESH | Occupational exposure limits |
| Pesticides | EU plant protection products, MRLs, Brazil |
| Cosmetics | EU Regulation 1223/2009, CosIng, SCCS opinions, UK rules |
Compare glyphosate's acceptable daily intake across the EU, US EPA, Codex, Japan and Korea in one question. See current coverage, including fashion and biocides.
How regulatory intelligence tools compare
Start with access and price. Can you put a real question through the tool today?
| Buying decision | RegAffairs AI | Published sales route |
|---|---|---|
| Know the price before a call | Free to try; see pricing | Enhesa: talk with the team for a tailored quote |
| Try a question today | Self-serve access, no demo call | CUBE: book a demo |
With RegAffairs AI, your first question returns cited claims and a research trail you can inspect.
Who uses a regulatory intelligence tool like this
- In-house regulatory affairs and product stewardship at chemical, coatings, ink and agrochemical manufacturers. They ask questions like What does REACH Article 33 require for SVHCs in articles, and how does SCIP notification work?
- Only Representatives run lookups for dozens of clients: which national inventories list a CAS number, and whether it is on a restriction or authorisation list.
- SDS authors check a line before they write it. What is the regulatory status of HBCDD in the EU, the US and China? is one search, not three.
- Pharma regulatory affairs can start from What are the GMP requirements for drugs in Canada under Part C Division 2?
- Food, cosmetics and pesticide teams ask Which phthalates are restricted in cosmetics, and under which annex entries? or about the acceptable daily intake for glyphosate across the EU, US EPA, Codex, Japan and Korea.
- Consultancies use it for the first pass before the consultant, then spend billable hours on judgment.
Read public answers to see the citations before you ask your own.
Regulatory intelligence software pricing
Free to try; Pro costs $100 per user per month.
- Free: no credit card. The full corpus, all jurisdictions, cited answers and the research trail.
- Pro: unlimited questions, deep research and priority speed. Month to month, cancel anytime.
- Enterprise: seats, SSO and procurement on request.
See plans and start without booking a call.
Built for regulated teams
Your questions, documents and uploads are never used to train models. Data is processed and stored in the EU by default. Every answer carries its research trail, so a colleague can retrace it. Details are on the security page and in the FAQ.
FAQ
What is regulatory intelligence software?
It tells you what regulators require of your substances, products and markets, and what is changing. RegAffairs AI answers your question from official regulatory text, with a citation on every claim.
How is RegAffairs AI different from other regulatory intelligence tools?
You get an answer, not a list of hits. Every claim links to the stored source, and you can start free today with no demo call.
Where do the answers come from?
Official regulatory sources, including ECHA, FDA, EMA and national regulators. Explore the coverage for your next question.
Ask your first question
Type a CAS number, or the question you would otherwise send a colleague, and read the cited answer. Try it free. No credit card and no demo call.