Medical Device Regulation (MDR) Technical Analysis and Documentation: Gain expertise in preparing and managing technical documentation for MDR compliance.
Learning Objectives
- Learn the technical requirements of MDR compliance.
- Develop skills in creating technical documentation.
- Understand conformity assessment and risk analysis processes.
- Ensure compliance with MDR for product safety.
- Improve technical documentation quality and accuracy.
Framework Connections
The materials within this course focus on the NICE Framework Task, Knowledge, and Skill statements identified within the indicated NICE Framework component(s):
Competency Areas
Feedback
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