- Module 1: Introduction to the EU IVDR
- History & Purpose of the EU IVDR
- Structure & Scope of the EU IVDR
- Key Sections & Terminology under the EU IVDR
- Key Changes & Timelines for Transition
- Module 2: Some Key Aspects of the EU IVDR
- Devices covered under the EU-IVDR
- Devices in scope and out of scope
- Brief Overview of Economic Operators & Health Institutions, Principles of Classification & Conformity Annexes
Our FREE EU IVDR 2017 746 Training (Essentials Training Course) is aimed at 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 Online EU IVDR 2017 746 Essentials Training Course is most definitely for you!
On completion, successful Learners will have the knowledge needed to:
Successful completion will entitle each Learner to receive a digital Certificate of Completion.
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
In order to successfully complete FREE Online EU IVDR 2017 746 Essentials eLearning course, each Learner will need to:
- Complete the course modules and obtain 70% or higher in the final assessment (MCQ-based)
Upon registering for this course, each Learner will have 30-days of eLearning access to complete the course.
There are recommended requirements for each Learner in wishing to complete any of our eLearning modules. In our experience, Workplace IT environments’ internal configurations and available software can vary (new or old), and there may be various limitations or other restrictions in place, and as such, the functionality of any Learning Management System (LMS) may be impacted, restricted and may not perform well.
Click here to read the full technology requirements.
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