The ability to access and collaborate with a research site is essential to the success of every study. Each phase and clinical operations process requires the ability to access, review, and exchange documents efficiently and promptly.
A disconnected mix of on-site visits, email communications, and portals restrict site access and document exchange for Sponsors and CROs alike.
What has changed? Sites are making significant investments in purpose-built electronic Investigator Site File (eISF) platforms to streamline their internal operations, with 63% of all sites planning to have an eISF in place by the end of 2020.
As study sites “come on-line,” Sponsors and CROs are in a unique position to harness this electronically connected network of sites to turn on remote site access, Source document review/verifi cation (SDR/V), and “and streamlined workflows.
Florence is on the leading edge of innovation and transformation, currently powering over 7,200 sites with its eBinders platform for eRegulatory and is connecting Sponsors and CROs to their sites via Florence eHub for remote monitoring.
Florence eHub is a collaborative workspace, providing unprecedented levels of remote site access and document quality control that ultimately decreases study cycle times while increasing data quality.
In this whitepaper, we examine the study processes that Florence eHub accelerates.