The new EU MDR represents a considerable change from the directives it replaced. During this course, you will learn about the new requirements in the EU Medical Device Regulation (MDR), including those related to quality systems, product classification rules, technical documentation, clinical evaluations, Unique Device Identification (UDI), and postmarket surveillance.
You will also learn how to plan an efficient implementation of the new regulation.
The British Academy for Training and Development offers this course to the following categories:
After completing the program, participants will be able to master the following topics:
Note / Price varies according to the selected city
Maintenance of Medical Devices and Identification of Faults
2024-10-07
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