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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:
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.
On completion, you'll be awarded an internationally recognized BSI Training Academy certificate
If you have any enquiries, let us know how can we help you.
Call: +91 80815 80815
Email us: info.in@bsigroup.com
Reach out and see how we can help guide you on your path to sustainable operational success.