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Understanding the CE Marking process for Medical Devices – 1 day course

What you will know by the end of the course:

The course will give you a wide understanding of the Medical Device Directive (MDR (EU) 2017/745) and how it applies to your medical device application.

Following the course, you will understand how to fulfil the Essential Requirements and how to create a compliant product Technical File.


Contact us today to see how we might help you!.