EU MDR 2017/745 Training (PART I): Introduction
Welcome to an Introduction to European Union Medical Device Regulations 2017/745. This module is an introductory module to explain how, why and when the new regulations have come into force, what they consist of and some of the new and strengthened features. We will look at some of the historical events that have occurred over a period of decades and their consequences and we will be able to see the triggers for changes in legislation and understand what brought these changes about. This module includes a high-level overview of the contents of EU MDR 2017/745, some of the new features, the timelines for compliance and we’ll take a look at how the new MDRs compare to MDD.
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- By Yuval Shapiro
Module 1: EU MDR 2017/745 Training - Chapter I - Scope and Definitions
Chapter I - Scope and Definitions comprises four articles that lay the basis for the regulations
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- By Yuval Shapiro
Module 2: EU MDR 2017/745 - Chapter II - Making Available on the Market
EU MDR 2017/745 - Chapter II - Making Available on the Market
- Course
- By Yuval Shapiro