The market-leading medical device regulatory intelligence software. Every safety alert, regulatory change, and market signal aggregated from 27 regulators and delivered in under 90 seconds.
We parse 27 regulatory bodies, 140,000+ signals every month — classifying each as safety alert, regulatory change, market trend, clinical update, or supply event. No PDFs to skim. No RSS to babysit.
Pin every regulatory signal to the city it affects. See where an event landed, how many devices are exposed, and the nearest supply-chain risk.
Insights on medical device regulations, compliance, and market trends.
FDA launched AEMS in March 2026 to replace MAUDE, FAERS & 5 other databases. What changes for medical device teams — new features, timeline, API migration & what stays the same.
Read more →How to search FDA MAUDE (transitioning to AEMS May 2026). MDR reporting rules, 5-day reports, openFDA API, event types & real-time monitoring. Free tool included.
Read more →Step-by-step guide to transitioning from MDD to EU MDR — extended deadlines, legacy device rules, Notified Body capacity, technical documentation gaps & re-certification strategies.
Read more →Free forever · No credit card · All 27 regulators