Article | February 22, 2023

Automate The Protocol With eSource

Source: CRIO

By Raymond Nomizu, CEO at CRIO

GettyImages-1435078862 esource

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.

access the Article!

Get unlimited access to:

Trend and Thought Leadership Articles
Case Studies & White Papers
Extensive Product Database
Members-Only Premium Content
Welcome Back! Please Log In to Continue. X

Enter your credentials below to log in. Not yet a member of Clinical Leader? Subscribe today.

Subscribe to Clinical Leader X

Please enter your email address and create a password to access the full content, Or log in to your account to continue.


Subscribe to Clinical Leader