In-Vitro Diagnostic Reporting (IVDR) Overview Training

This course is an overview of the IVDR regulation. Gain an understanding of the purpose, approach, and requirements an audit program, and its benefits to medical device manufacturers. Have your questions answered.

Course topics:

• What is IVDR?
• How does IVDR work?
• How does IVR fit with other requirements?

Upon successful completion, learners will:

• Understand the objectives, requirements and structure of IVDR
• Recognize its relationship with other requirements
• Describe the IVDR process
• Explain the benefits of IVDR for medical device manufacturers

This course is intended for auditors of medical device manufacturers and anyone in the medical device industry who wants to gain an understanding of IVDR. 

Learners attending the virtual training option require hardware, internet connection and audio connection for the full duration of the course.