Medical Device Adverse Events – Reports, Trends & Email Notifications | Never Use FDA MAUDE Again!
When: Wednesday, November 15, 2017 – Noon EST
This webinar will demonstrate how Device Events can be used by healthcare organizations to quickly and affordably identify, analyze and track, the health risks associated with specific medical devices before recalls are announced.
Attendees will see how the system can enable them to:
• Improve health outcomes and patient safety
• Inform procurement
• Reduce risks for their organizations
