EU IVDR Training #separator_sa In Vitro Diagnostic Regulation

Online EU IVDR 2017 746 Essentials Training

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Online EU IVDR Training for anyone working in the medical device industry sector who is looking to understand the basic essentials of the European In Vitro Diagnostic Regulation (EU IVDR 2017 746). If you are not 100% sure or would like to refresh your knowledge, then our online course is most definitely for you!

Our 2hr eLearning course is a highly interactive way to learn at a time & a pace that works best for you, making it easier to get the training you need while balancing a busy home or work life.

Subject Area
Medical Devices
2 Hours
Contact Sales
Comply Guru

Learning Objectives

On completion of this Online EU IVDR Training Course, successful Learners will have the knowledge needed to:

  1. Explain the history, purpose, and structure of the EU IVDR
  2. Describe the key changes to the EU IVDR from the IVDD
  3. Explain what an IVD medical device is
  4. Describe the types of IVD devices that are covered by the regulation
  5. Outline some other key aspects of the new EU IVDR

Course Content

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Who should attend?

    • Anyone working in the Medical Device Industry
    • Anyone interested in a brief overview of the EU IVDR.
    • Quality assurance professionals
    • Quality Engineers
    • Research and Design Engineers
    • Internal Auditors
    • Quality Managers
    • Manufacturing Engineers
    • Regulatory professionals

Note: EU IVDR 2017 746 Essentials Training is not just for Regulatory Professionals and is a suitable course for anyone wishing to gain a general overview of the EU IVDR.

Assessment & Certification

Assessment Methodology

In order to successfully complete this course, each Learner will need to:

  • Complete all eLearning modules and obtain 70% or higher in the final assessment (MCQ-based)


Successful completion will entitle each Learner to receive a digital Certificate of Completion.