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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.
BSI에 문의하여 지속 가능한 성공적인 운영 방침을 알아보세요.