Moving to an eRegulatory/eSource solution generates measurable impact on clinical trial study startup timelines. Research teams reduce startup time by as much as 40% through harnessing the built-in features of eBinders combined with excellent standard operating procedures.
Below are the top ten features more than 3,000 research teams are using to accelerate their study startup timelines and more efficiently manage their regulatory and source workflows.
For a consultation on how Florence can help your team optimize study startup with a purpose-built eRegulatory and eSource solution get in touch today.
Learn More About Florence eBinders
Florence eBinders is the leading eRegulatory and eSource solution trusted by more than 3,000 clinical research teams around the world. To setup your consultation and discover how Florence can accelerate your study startup timelines, as well as optimize your document workflows and enable remote monitoring, get in touch today!