Course Description
Two day training on the Medical Device Regulation (MDR) 2017/745 to provide Medical Device Manufactures an overview of the MDR. Objectives of the course are:
Understand the basic requirements of the Medical Device regulation (MDR) 2017/745
Understand similarities of the MDD to the MDR “process”
Learn to navigate the MDR document
Review new MDR requirements
Know what to do to comply with CE-marking requirements per the Medical Device Directive (yes the MDD) and the MDR today and tomorrow
Prepare for significant changes
Know where to go for guidance