Requirements for Risk Classification EU MDR 2017/745 On-demand training

Level Requirements Duration 1 hours

Available to book: Public classroom View dates and book now

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 eLearning course, You’ll have access to the course for 12 months.

Please Note: This training fee is applicable only for residents of India and the Indian subcontinent.
This is an online, interactive eLearning course, You’ll have access to the course for 12 months.

Please Note: This training fee is applicable only for residents of India and the Indian subcontinent.
This is an online, interactive eLearning course, You’ll have access to the course for 12 months.

Please Note: This training fee is applicable only for residents of India and the Indian subcontinent.

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