Your cybersecurity, privacy, AI, and medical device rules, mapped in minutes
The Qity Compliance Radar shows which EU and UK cybersecurity laws, data protection rules, product safety duties, and AI Act requirements apply to your company. Tell us your size, markets, sector, and what you build, and see what is law today, what starts on a known date, and which standards and certifications your buyers will ask for. If you make a medical device or an IVD, the Radar also classifies it across 17 markets.
No account, no email required to see your results.
Choose your depth
The first three routes build on each other: each one asks everything the shorter route asks, and more. The fourth classifies a medical device or an IVD in the markets you choose.
One minute scan
About 1 minute
Your organisation only: where you are, how big you are, what sector you are in, and whether you touch personal data, software, or AI.
- 8 to 10 questions, no product detail
- The headline laws that apply to your organisation
- A first, practical security baseline to aim for
Quick scan
About 5 minutes
Everything in the one minute scan, plus the horizontal picture across data protection, network security, product security, and AI.
- About 15 questions
- Cross-sector laws and dated future obligations
- Good enough to brief a board
In-depth mapping
15 to 20 minutes
Everything in the quick scan, plus sector and product depth: market access, supply chain, transfers, resilience, and the standards behind your conformity route.
- Sector-specific and product-specific obligations
- Country-level and product-category branching
Device classification
About 5 minutes per market
Find out whether your product is a medical device or an IVD, which risk class it falls in and under which rule, and what follows, for the markets you choose.
- Qualification, class, and the rule cited
- Software, and how the AI Act fits in
- 17 markets, including the EU, UK, and US