Medical device
regulatory data
infrastructure
for the world.
We collect, process, and deliver regulatory intelligence from 27 global regulators in real time. Powering products like MedFlux and enterprise API clients with 140,000+ signals per month.
Every regulator.
One data platform.
We parse 27 regulatory bodies, 140,000+ signals every month — classifying each as safety alert, regulatory change, market trend, clinical update, or supply event. Raw data, structured APIs, real-time delivery.
Data products
built for the industry.
Real-time regulatory intelligence terminal for medical device professionals. Six modules, one live dataset. Free tier available.
Try MedFlux Free →Programmatic access to our regulatory intelligence dataset. Real-time feeds, historical archives, and structured queries for enterprise integration.
Contact for API Access →Built for enterprise reliability.
Our data pipeline runs 24/7 with redundant infrastructure and automated failover.
Comprehensive coverage across FDA, EMA, NMPA, PMDA, MHRA, TGA, and 21 more agencies.
From regulatory publication to your dashboard in under 90 seconds.
We follow industry best practices for data handling, security, and privacy. Working toward SOC 2 and GDPR compliance.
Your data layer
for regulatory intelligence.
Try MedFlux free · Enterprise API available · 27 regulators covered