Program Description

Device Research & Regulatory Webinar Series 

Goal: This medical device webinar series will feature 3 sessions and 3 experts presenting topics to assist those in roles specific to medical device design, development, testing, analysis, and post market management. 

Learning Objectives: Upon completion of this course the attendee should be able to:

  • Describe the basic overview of the regulatory framework for medical device research and development 
  • Discuss the history and meaning of Broad Consent
  • Discuss billing and reimbursement for different types of device trials