London, 2024-05-18
Training Course in Implementing the EU’s Medical Device Regulation
Summary | 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. |
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Objectives and target group | 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:
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Course Content |
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