Online EU IVDR 2017 746 Essentials Training

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

• 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.

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

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.