Basis of European Regulatory Affairs for in vitro Diagnostic Medical Devices Current Status Not Enrolled Price CHF70 Get Started orLogin Gain a fundamental insight into the new European regulatory framework for in vitro diagnostic medical devices focusing on legal basis Course Content Expand All Chapter 1: European Regulatory Framework-IVD 4 Topics | 1 Quiz Expand Lesson Content 0% Complete 0/4 Steps What is Regulatory Affairs? European Legal Basis European Regulatory Trend-IVD CE Marking-IVDR Quiz_ European Regulatory Framework Chapter 2: Classification of in vitro Diagnostic Medical Devices 9 Topics | 1 Quiz Expand Lesson Content 0% Complete 0/9 Steps Definitions Impact of Classification Classification Rules Classification Flow Practical Example: Classification of in vitro Diagnostic Medical Device Borderline Products Categories of Medical Device Software Classification Flow of Medical Device Software Practical Example: Classification of Medical Device Software Quiz_Classification of in vitro Diagnostic Medical Devices
