Regulatory intelligence for teams who cannot check 27 websites every morning
MedFlux is a market intelligence terminal for medical device professionals. We aggregate safety alerts, regulatory changes, and market signals across 27 authorities and deliver them in under 90 seconds — with free tools, deep educational content, and transparent editorial standards.
WHO WE SERVE
Regulatory affairs, quality, post-market surveillance, and market access teams at device manufacturers, suppliers, and consultants. If your job depends on catching an FDA recall, NMPA update, or EU MDR change before it becomes a crisis, MedFlux is built for you.
WHAT WE BELIEVE
- People-first content over doorway pages — we prune thin programmatic URLs rather than inflate sitemaps.
- Primary sources — FDA, EUR-Lex, PMDA, NMPA and other official references are cited on deep pages.
- Free forever utility — recall lookup, 510(k) predicate finder, and Japan pathfinder stay free because they create real workflow value.
EDITORIAL BOARD
Named editorial personas review regulatory explainers and glossary depth. Bios describe domain expertise used to shape content. For standards on sourcing and corrections, see our editorial policy.
Ehemaliger leitender Auditor einer benannten Stelle mit mehr als 15 Jahren Erfahrung in der EU-MDR/IVDR-Implementierung.
EU MDR · IVDR · ISO 13485 · Clinical Evaluation
Experte für NMPA- (China) und PMDA-Registrierungswege (Japan). Spezialisiert auf grenzüberschreitende Harmonisierung.
NMPA · PMDA · CDSCO · TGA
Spezialisiert auf FDA 510(k)-Einreichungen, De Novo-Wege und Quality System Regulation (21 CFR 820).
FDA · 510(k) · PMA · 21 CFR 820
COMPANY
MedFlux is a product of Adventurer Limited. Product application: app.medflux.live. Demo: book a walkthrough.