Massive amounts of data are collected, analyzed, and reported to different audiences during a clinical trial. While gathering this data is necessary and critical, how can we prevent being overwhelmed by its sheer quantity and not miss out on important operational indicators that make running trials more efficient?
Watch Jason Methia, VP site strategy at Veeva, discuss strategies that reduce information overload and simplify how sites, sponsors, and CROs work together throughout the clinical trial process.
- How to measure and benchmark trial performance
- Best practices for driving greater efficiency and collaboration
- Strategies that reduce information overload in research