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.
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