The Values and Benefits of Medical Device Reporting Compliance 2015
07 Apr 2015
Webinar
Key Topics
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
Who should Attend
Quality and Regulatory Specialists
Quality and Regulatory Managers
CAPA Coordinators
Complaint/MDR Coordinators
Hospitals and Long Term Care Facilities
Medical Device Importers
Pharmacies
Past Events
The Values and Benefits of Medical Device Reporting Compliance 2015 - 07 Apr 2015, Webinar (50684)
The Values and Benefits of Medical Device Reporting Compliance 2026
Important
Please, check "The Values and Benefits of Medical Device Reporting Compliance" official website for possible changes, before making any traveling arrangements
