• Online, Self-Paced
Course Description

Introduction to Medical Device Regulation (MDR) Compliance: A foundational course to navigate regulatory compliance under the MDR framework for medical devices.

Learning Objectives

  • Understand the key principles of MDR compliance.
  • Learn the regulatory pathways for medical devices.
  • Develop skills in MDR documentation and submission.
  • Identify risks and implement regulatory strategies.
  • Ensure product safety and compliance with MDR.

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