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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.
On-demand - training that’s even more flexible
This short course aims to give you a better understanding of the Risk Classification requirements as per the EU MDR (2017/745). We discuss why there is a need to classify, the importance of stating the intended purpose and how this plays a role in applying the correct conformity assessment procedures.
This course will help you:
By the end of the course, you will be able to:
Quality, Regulatory, Technical professionals working in the Medical Device industry
On completion, you’ll be awarded an internationally recognized BSI Training Academy certificate.
Explore our BSI Academy knowledge bundles, giving you great savings across multiple courses and an opportunity to maximize your training budget.
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