Atlantic Research Group (ARG), IACT Health, and Veeva Systems will discuss the industry perspective on data sharing and collaboration in clinical research, the use of metrics to optimize performance, and strategies that reduce information overload and simplify how sites, sponsors, and CROs work together throughout the clinical trial process.

This session will cover identifying, assessing, and reporting adverse events (AEs) for medical device studies at the site level.

This presentation will focus on lessons learned from a recent observational study of 6 clinical research sites over the course of three years.