Clinical Research Sites today must scale their processes to manage increasing study demand and protocol complexity.
eRegulatory is the natural first step in implementing scalable and compliant processes. However, workflow complexities of clinical research can often hinder adoption of digital tools.
After hundreds of clinical research site eBinder implementations, our team has assembled this free guide of Best Practices for eRegulatory Transition.
The Clinical Research Roadmap to eRegulatory
Discover the Best Practices to an eRegulatory Transition
"Florence's eBinder Suite has transformed the typical “ask and response” workflow process by developing an investigator site file during startup that has a shared sense of responsibility."
What Sites are saying about Florence
We manage multi-center studies and eBinders gives us the power to be several places at once. It works really well for remote regulatory document review and enrollment approvals, and as a result gets sites up and running quickly.
Melissa M. Bolton
Research Program Coordinator
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Download the Clinical Research Roadmap to eRegulatory