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