Career
7
Contact us
Career
7
Contact us

MDR & CE Marking Process

Understanding European legislation and the expectations of the authorities is crucial for getting a device on the European market. This course will provide a solid understanding of the content of MDR legislation, starting with the basic definitions of a medical device, classification, conformity process, general obligations of the manufacturer, General Safety and Performance Requirements, Clinical Evaluation/Investigations, UDI, and other key content.

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Do you want to know more about Finished Products Engineering?
Do you want to know more Process Engineers?
Do you want to know more Medical Device & QA?
Do you want to know more about Finished Products Engineering?
Do you want to know more Process Engineers?
Do you want to know more Medical Device & QA?