• Online, Self-Paced

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