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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 various economic operators and their obligations according to the MDR.
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.
Reach out and see how we can help guide you on your path to sustainable operational success.