From Left: Stan Saylor, Edquina Washington, Keith Gillespie, Madris Tomes, Chris Reilly, Sandie Walker
About Device Events
Device Events is an online software service that provides easy retrieval of adverse event reports from FDA MAUDE, Global UDI (GUDID) and RECALL databases so users can proactively identify problem medical devices and take appropriate and timely action. Healthcare organizations, insurance companies, manufacturers, and patient advocacy groups alike can use Device Events to quickly identify problematic devices, before any FDA action, to improve patient safety and health outcomes, strengthen risk management, reduce liability, and save time and cost across their organization. For more information visit our website at www.deviceevents.com
|