Regulatory compliance software for products and substances
RegAffairs AI is regulatory compliance software that answers your product or substance question in seconds, with every claim linked to its source.
No more digging through scattered registers. Start self-serve, free to try.
Try it free. No credit card or demo call.
Ask whether a substance, ingredient or product can be sold in a market. Ask what restrictions, labels, registrations or deadlines apply. RegAffairs AI searches official regulatory text and shows the research trail beside the answer. Your team can open the evidence before forwarding it to legal or a customer.
Regulatory compliance software that answers the compliance question
A launch or reformulation starts with specific questions:
- Status: Is this substance listed, restricted or authorised? What changed after the last amendment or court ruling?
- Market requirements: What thresholds, triggers and language duties apply in the EU, UK and US? Who holds the registration?
- Obligations: Who has to notify, by when, and under which article?
Ask across jurisdictions in one question. The answer brings together history, current text and case law. Duty holders and deadlines come from the operative text, so you can check the article behind each requirement.
See a worked example: What is the regulatory status of BPA in Canada? The answers page has more questions to try.
How automated regulatory compliance software handles research
- Ask your question in plain language, in your own language. Add a CAS number, ingredient, product type or market to focus it.
- The agent reads the sources. It searches official registers and reads the operative text. Quick answers arrive in seconds. Pro's deep research mode works through multi-step, multi-market questions.
- Open the evidence. Every claim links to its stored source document. The page shows every search and document the agent read.
The searches, the reading and the cited answer all run from your question. See the method in cite the paragraph.
What the best regulatory compliance software does for product teams
Test product compliance software with a question your team received this week. Can you open the source behind the answer? Can legal follow the research without repeating it?
RegAffairs AI gives you:
- Source-backed answers: citations open official regulatory text, including annex entries and register records.
- Cross-jurisdiction research: compare requirements in covered markets in one question.
- A visible research trail: review the searches and documents behind each answer.
- Weekly updates: the corpus is refreshed weekly, with new sources added every week.
- Day-one access: ask without an implementation project, data load or templates.
- Public pricing: start free, then choose Pro.
Start with an answer, not a sales call
| Access and pricing | RegAffairs AI | Published vendor entry points |
|---|---|---|
| First step | Ask a question self-serve, free to try, no credit card | Assent leads with "Book a demo"; Enhesa invites you to schedule a call |
| Price before a call | Public Pro price | Enhesa provides a tailored quote after discussing scope with its team |
Regulatory compliance software coverage for your industry
Search official sources across chemicals, pharma, food, cosmetics, pesticides, biocides, ESH and fashion as one corpus. The coverage list shows the registers and markets.
- Chemicals: ECHA REACH and CLP, SVHC, Annex XIV and XVII, the C&L inventory, US TSCA, UK REACH and Turkey KKDIK.
- Pharma: EMA, FDA and national medicines regulators.
- Food: EU additives, contaminants, FIC and health claims.
- Cosmetics: EU Regulation 1223/2009, CosIng and SCCS opinions.
- Pesticides: EU plant protection products, MRLs and Brazilian sources.
- ESH: occupational exposure limits.
Explore biocides and fashion coverage too. Comparing chemical compliance software? Start with a CAS number and the markets you sell into. New sources are added weekly, and you can request a source.
Put your next compliance check to work
- Product stewardship teams and Only Representatives can compare HBCDD's status in the EU, US and China.
- SDS authors can check classification, restriction and inventory records before writing the sheet.
- Article suppliers can open the answer on REACH Article 33 and SCIP notification.
- Pharma teams can start with Canada's drug GMP requirements.
- Ingredient checks include phthalates restricted in cosmetics and glyphosate acceptable daily intake across markets.
- Consultancies can use the same cited research for the first pass before the consultant.
Regulatory compliance software pricing: free to try
The Free plan includes the full corpus, all covered jurisdictions, cited answers and the research trail, with no credit card. Pro is $100 per user per month, with unlimited questions under fair use, deep research and priority speed. It is month to month, and you can cancel anytime.
Enterprise seats, SSO and procurement are available on request. Questions, documents and uploads are never used to train models. Data is processed and stored in the EU by default. See security.
FAQ
What is regulatory compliance software for products and substances?
It answers whether a substance, ingredient or product can be sold in a market, and what obligations apply. RegAffairs AI answers from official regulatory text, with citations you can open.
What makes it the best regulatory compliance software for a small team?
You start today without an implementation or demo call. Ask a plain-language question across covered markets and get a cited answer to show legal or a customer.
Is this automated regulatory compliance software?
Yes: the regulatory research is automated. The agent searches official registers, reads the text and writes a cited answer.
Check your first product or substance
Take the CAS number or ingredient waiting in your inbox. Ask what applies, open the sources and share the research trail.
Try it free. No credit card. No demo call.