The Values and Benefits of Medical Device Reporting Compliance 2015 is a webinar that covers topics such as:
- Consequences for Non-Reporting and Over-Reporting
- Medical Device Reporting History, Overview, and Basics
- When do malfunctions need to be reported?
- Definitions: Serious Injury, Death, Malfunction, User Error, Reportable Event
- MDR for Manufacturers and Importers
- The eMDR System
- The MAUDE Database
- MDR for User Facilities
The Values and Benefits of Medical Device Reporting Compliance 2015 is intended for:
- Quality and Regulatory Specialists
- Quality and Regulatory Managers
- CAPA Coordinators
- Complaint/MDR Coordinators
- Hospitals and Long Term Care Facilities
- Medical Device Importers
- Pharmacies
