4 articles
Search the FDA MAUDE database for medical device adverse event reports. How to query MAUDE, understand MDR reporting under 21 CFR 803, use the openFDA API, and set up real-time monitoring.
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.
Search and monitor FDA medical device recalls in real time — Class I/II/III lookup via openFDA API, automated alerts, MAUDE integration & free recall search tool.
How top medical device companies use real-time regulatory intelligence to catch FDA, EMA & NMPA changes 10x faster. Practical framework for RA teams with tool comparison.