Basis of European Regulatory Affairs for in vitro Diagnostic Medical Devices Current Status Not Enrolled Price CHF70 Get Started 要么Login Gain a fundamental insight into the new European regulatory framework for in vitro diagnostic medical devices focusing on legal basis 课程内容 展开全部 Chapter 1: European Regulatory Framework-IVD 4 主题 | 1 测验 Expand 课内容 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 主题 | 1 测验 Expand 课内容 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
