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United StatesComply Guru offer a European Medical Device Regulation (EU MDR 2017/745) Essentials Course for organizations looking for a concise, high-level introduction for their staff.
Our 2hr Essentials training courses are 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.
Why Comply Guru?
- Self-Paced, On-Demand Learning (24/7)
- Highly Interactive, Engaging Experience
- Industry-leading Methodology
- Designed by Experts with Proven Expertise
Course Overview
EU MDR 2017/745 Essentials
Explain the history, purpose, and structure of the EU MDR
Describe the key changes to the EU MDR from the MDD
Identify the different roles and responsibilities associated with the EU MDR
Outline the requirements for placing a medical device on the market
This course is for organizations who wish to provide their staff with a short, general overview of the EU MDR.
Successful completion will entitle each Learner to receive a digital Certificate of Completion.
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)
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 the full technology requirements here.
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