Streamline clinical trials

Florence’s product suite enables researchers and sponsors to manage the administrative tasks
of clinical trials with significantly more efficiency and seamless compliance within FDA, HIPAA
and Part 11 guidelines. The eBinder product allows on-site researchers to execute documents
digitally, store and populate forms with embedded compliance flags, and share a uniform dataset
across the study via cloud-based software – tasks that collectively comprised dozens of hours per
week per researcher. Florence can also provide similar efficiencies to the sponsor/CRO side of
the network via the eHub product, the remote monitoring tool used by centralized trial sponsor
teams that otherwise would fly on-site to review paper study binders with disparate datasets.


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