Awareness of the Medical Device Regulation (MDR) Training Course - eLearning

Stufe Grundlagen Dauer 0.5 Stunden

Verfügbar zur Buchung:: On-Demand-E-Learning €40 Book now

The Medical Device Regulation (MDR) is a comprehensive set of European Union (EU) rules that govern the production, sale, and distribution of medical devices. These devices play a crucial role in diagnosing, monitoring, preventing, and treating medical conditions, ensuring they meet the highest standards of safety and performance. This short course will focus on how the MDR prioritizes safety, effectiveness, and the highest standards of public health within the EU.

How will I benefit?

This course will help you:

Understand the regulatory framework for Medical Devices in Europe
Recognize the commercial advantages of obtaining the CE Mark as evidence of conformity with the Medical Device Regulation (MDR)
Identify actionable steps you can take to ensure compliance with the MDR and how it can benefit you

Please note: The eLearning training lasts approximately 30-60 minutes and is in English.

Benefits of On-Demand for the individual

Convenient - courses are available 24/7 and you can learn at any time and from any place that suits you – you just need an internet connection

Learning pace - You can learn as fast or as slowly as you want to. You can also take breaks at any time in the course and pick up where you left off when you are ready to continue

Information retention - During the access period, you can go back and repeat parts or all the course to refresh and reinforce what you have learned

High-quality materials - Developed by top subject matter experts, course content is both detailed and engaging, with explanations, activities, and knowledge checks to enhance your learning

Upon completion of this course, you will be able to:
- Explain how Medical Devices are regulated in Europe
- Describe the commercial benefits of the CE Mark demonstrating conformity with the Medical Device Regulation (MDR)
- Suggest actions you can take to help with compliance to the MDR
All staff in medical device organizations.
On successful completion of the training, participants will receive an internationally recognized certificate

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