Automate The Protocol With eSource

By Raymond Nomizu, CEO at CRIO

Compiling source data is still mostly paper-bound in the clinical research industry and is often the cause of great inefficiencies in research today. By automating this one process, clinical teams could drive 20% cost savings, drastically reduce protocol deviations, improve patient safety, virtually eliminate audit risk, and hasten speed to market.

So, how is a paper-based process automated? Discover how a combination of protocol execution by sites and CRIO’s site-based eSource is presenting a huge and ready-made opportunity for sponsors to conduct clinical trials more efficiently.