Shifting to eRegulatory and eSource workflows is a requirement for clinical trial sites to continue to scale and grow their studies.
However, many site leaders are not fully prepared for the transition.
With over 6,200 clinical trial sites and sponsors now active in Florence eBinders, we have compiled this Guide to eRegulatory and eSource to assist trial sites in understanding important information when considering these technologies.
This guide is designed as an in-depth overview of how eRegulatory and eSource are impacting Clinical Trials, and the steps you can take to prepare now.
Continue to be at the forefront of innovation in Clinical Research.