Description

Delegates participating in this course will:

  • Gain an overview of the critical changes with EU MDR and EU IVDR, and their implications
  • Find out about implementation timescales and their impact on resources
  • Discover what EU MDR and EU IVDR mean in practice

Objectives

About the EU MDR and EU IVDR


The EU MDR and EU IVDR were published in the Official Journal of the European Union on May 5, 2017 as Regulation (EU) 2017/745 and Regulation EU (2017/746). The new rules will apply after a transition period of three years for MDR and five years for IVDR. These two eLearning courses will help medical device and In Vitro diagnostic device manufacturers understand the complex new regulations.

Audience

This course is intended for, but not limited to, regulatory personnel, managers, CEO, CFO, or any medical device or IVD field personnel who want to learn about the new regulations.


Bundle Components

Choose an offering for each one of the bundle components then click on 'Add To Cart' button below:

Introduction to the New EU Medical Device Regulation (MDR) eLearning Course

Offerings

Introduction to the New EU Medical Device Regulation (MDR) eLearning Course

Introduction to the New EU In Vitro Diagnostic Regulation (IVDR) eLearning Course

Offerings

Introduction to the New EU In Vitro Diagnostic Regulation (IVDR) eLearning Course

View Details

44323318

THB 11590 THB 9492 Excluding VAT

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