Prioritizing eReg Site-Centric Workflows Within A Connected Research Ecosystem

The Challenge

To conduct compliant and efficient research, sponsors and CROs were early adopters of clinical research technology. However, as adoption of clinical research technology increased, more sites began to utilize technology built to support their own studies and workflows. The lack of connectivity and collaboration between sponsors and sites who own and want to use their own technology has resulted in duplicative workflows, imposed new processes, and increased administrative burden. Due to their high volume of research across industry- and investigator-initiated studies, site staff at Duke University experienced the impact of these inefficient processes on an exponential level.