Webinar Replay: Best of ACRP 2018: Adverse Event Reporting in Medical Device Trials: Requirements from a Monitoring and Auditing Perspective

This session will cover adverse event (AE) reporting for medical device clinical trials, including the following topics: the differences between pharmaceutical and device AE reporting requirements, how to understand the AE reporting requirements for device trials based on a study protocol, and a discussion on device AE reporting requirements from a monitoring and auditing mindset. Webinar replay expires on November 13, 2019.