Built for medical device RA and quality teams who cannot wait on slow enterprise RI tools. MedFlux aggregates safety alerts, regulatory changes, and market signals from 27 authorities — free core access, under 90-second latency, plus free FDA tools.
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.
Traditional regulatory intelligence suites are powerful — and slow to buy. MedFlux is the fast path for device manufacturers, suppliers, and consultants who need global signal coverage today.
Coverage and workflows center on medical devices — recalls, vigilance, pathway changes, and competitor signals across device authorities worldwide.
Start without a procurement cycle. Use the intelligence feed free forever, plus open tools for FDA recalls and 510(k) predicate research.
Stop tab-hopping FDA, EUDAMED, NMPA, PMDA, TGA, and the rest each morning. One terminal, multi-language UI, signal classification included.
Deep MAUDE/AEMS, MDR, NMPA, and PMDA playbooks link into live monitoring so content and product reinforce each other.
Insights on medical device regulations, compliance, and market trends.
FDA Quality Management System Regulation (QMSR) took effect Feb 2, 2026. How Part 820 now incorporates ISO 13485:2016, CP 7382.850 replaces QSIT, and what RA/QA teams must do.
Read more →Free guide to searching FDA MAUDE & AEMS adverse event database. Learn 21 CFR 803 MDR rules, openFDA API Python queries, and real-time recall alerts.
Read more →Compare Japan PMDA vs US FDA medical device classification (Class I-IV), Shonin/Ninsho approvals, timeline, fees, and DMAL requirements. 2026 complete guide.
Read more →Academic Free for students. Demo for teams. Free public tools.
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.