innovative solutions
Looking for superior Search and Reporting alternative to MAUDE?
Device Events is a cloud-based software service that provides fast, easy-to-use, comprehensive and cost-effective access to the most up-to-date information on adverse events involving medical devices.
Who We Are
The
MAUDE
Solution
MAUDE – The Manufacturer and User Facility Device database platform is antiquated and difficult to use.
DEVICE EVENTS provides an alternative cloud-based software service that extracts, consolidates and provides clear and comprehensive metrics and reports on the millions of complex medical device adverse event reports (MDRs) and recalls that have been filed with the FDA.
Use the slider above to note changes between programs.
GET THE RIGHT DATA - USE DEVICE EVENTS.
Fast Search & Retrieve from the FDA MAUDE Database | Trend Visualizations | Email Notifications |
Signals is a Quarterly Newsletter on the latest medical device adverse event news, information and trends.
Would you like a demonstration of the unique features of our product? Please click the button below.
Fast Search & Retrieve from the FDA MAUDE Database | Trend Visualizations | Email Notifications |
Signals is a Quarterly Newsletter on the latest medical device adverse event news, information and trends.
Click below and view a quick 5 minute demonstration of key features of the Device Events Software.
GET THE RIGHT DATA - USE DEVICE EVENTS.
Software Features
Device Events is a cloud-based software service that extracts, consolidates, and provides comprehensive information on the millions of FDA medical device adverse event reports (MDRs). You can access the system at your convenience once you have account login credentials.
The system provides you with fast and cost-effective access to the most up-to-date information available – so you can quickly identify problem devices, understand the history, quantity and severity of the related adverse events and make better, more informed decisions.
The Device Events system will improve the quality of your research while reducing the amount of time you spend on that research. The result is improved patient safety, better health outcomes, and reduced risk for healthcare organizations.
association
Trusted
and
Supported
Former FDA Unique Device Identification (UDI) External Program Manager
Former FDA Adverse Events Project Manager for Devices (MAUDE)
Medical Device Epidemiology Network (MDEpiNet) UDI Think Tank
MDEpiNet National Medical Device Registry Task Force & Catalog Number Workgroup
