As study volume grows, here is the core issue – an increase in study volume and protocol complexity means a direct increase in task volume, but site resources are not increasing along the same rate. In fact, they’re not increasing at all (EP Vantage Analytics, 2017).
The Problem
Consequently, sites are being tasked with triple the work with the same amount resources and staff and budget.
The best research centers break above the workload logjam with technology: eRegulatory and eSource tools automate manual processes, reduce duplicate work, and standardize tasks in order to build predictability and increase compliance. Adopting these tools gives research teams the power to complete tasks more quickly and automate low level work so that they have more time to enroll and care for their patients. While the above benefits seem intuitive, the seasoned center manager should map out how such a tool helps in economic terms and build a return on investment (ROI) justification. We’ll explore exactly that here in a six part framework.
The Solution
The ROI of an eRegulatory Platform
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