This webinar is intended to help you get familiar with how to implement a medical device complaint handling system integrated with a unique device identification (UDI) system.
This webinar is further intended to provide actionable information and guidance on how to meet the regulatory requirements for handling any complaints concerning all medical device types including in vitro diagnostic medical devices.
This webinar is further intended to provide actionable information and guidance on how to meet the regulatory requirements for handling any complaints concerning all medical device types including in vitro diagnostic medical devices.
