Requirements - Risk Classification in the MDR (EU MDR 2017/745) - eLearning

Requirements for Risk Classification in the Medical Device Regulation (EU MDR 2017/745) - eLearning

Requirements - Risk Classification in the MDR (EU MDR 2017/745) - eLearning

Niveau Requirements (Eisen) Duur 1 hour

Beschikbaar om te boeken: On-demand elearning €60 Check prices and book

The Medical Devices Regulation (MDR) is the legislation detailing the requirements that manufacturers must meet to place medical devices on the market in the European Union.

Learn about the key requirements of risk classification under the MDR, gain a better understanding of the risk classification rules, the need to classify and why the intended purpose of a device is important.

How will I benefit?

This course will help you:

Appreciate the risk classification requirements as per the MDR
Gain an understanding of the risk classification rules with typical device examples

By the end of the course, you will be able to:
- Establish the requirements of Risk Classification as per the MDR Annex VIII
- Understand the medical device risk classification rules
- Appreciate the importance of the intended purpose driving the risk classification and selecting the appropriate conformity assessment procedure
Quality, Regulatory, Technical professionals working in the Medical Device industry
- This is an online, interactive on-demand course.
- The course content is both detailed and engaging, with explanations, activities, and knowledge checks to enhance your learning.
- Duration 1 hour
On completion, you’ll be awarded an internationally recognized BSI Training Academy certificate.

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