This two day course is designed for all levels of medical device professionals involved in the design and implementation of clinical trials.By the end of the course, participants will be able to: Describe the various types of medical device clinical trials; understand how clinical trial design impacts the promotion of a medical device; understand the regulatory requirements associated with device trials; describe the essentials of coordinating, monitoring, and managing a clinical trial with an emphasis on complying with Good Clinical Practices (GCPs) and understand how to develop a medical device clinical trial protocol and report.