Online EU IVDR 2017 746 Essentials Training
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!
Why Choose eLearning for EU IVDR Training?
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.
On completion of this Online EU IVDR Training Course, successful Learners will have the knowledge needed to:
- Explain the history, purpose, and structure of the EU IVDR
- Describe the key changes to the EU IVDR from the IVDD
- Explain what an IVD medical device is
- Describe the types of IVD devices that are covered by the regulation
- Outline some other key aspects of the new EU IVDR
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
EU IVDR Training Assessment Methodology
In order to successfully complete this eLearning course, each Learner will need to:
- Complete the course modules and obtain 70% or higher in the final assessment (MCQ-based) within the 30-day course license
EU IVDR Training Certification
Successful completion will entitle each Learner to receive a digital Certificate of Completion.
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. Read full technology requirements
Terms & Conditions
In registering for this course, each Learner and/or Customer expressly acknowledges that they have read, fully understood and agreed to be bound by all of Comply Guru’s terms & conditions, including additional licensing agreement. The terms & conditions & licensing agreement can be read here.
Reviews & Ratings
60 global ratings
Overall nice dashboard and mode of delivery...nice learning experience
IT's a good course because it makes you think on your feet. You need to thoroughly know the regulation before attempting the assessment.
Excellent E-learning experience!
Great over view- covered all of the important points.
Although I found this a bit tricky (after 30 years of no studying), I found it very worthwhile and extremely helpful.
Great course just enough detail to give basic understanding of IVDR
Very nice presentation with illustration and examples.
It was very informative course.
This course gives a good overview of what the EU-IVDR is without going into details about the actual requirements. A good starter.