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.