This session is presented by Clinical Research IO.
Sites have been adopting eSource for the past several years, as a natural extension of their steady technology adoption. Initially, eSource was thought of as a discreet, stand-alone category of software. But several recent trends point toward eSource becoming an actual platform for industry transformation.
Join experts from Clinical Research IO to explore how several independent trends in research will make eSource a platform technology for sites:
1. The adoption of de-centralized trials and virtual monitoring strategies by sponsors and CRO’s
2. The rising consolidation of site networks and integration of research into care settings
3. Integration with EDC, eConsent, and other technologies
Learn more about why eSource has such transformational power and how eSource will emerge as the backbone of research operations.
NOTE: This session does NOT offer ACRP Contact Hours.
The role eSource plays in facilitating virtual monitoring.
How technology facilitates consolidation of research site activity.
How to prepare your site for a new era of hybrid virtual trials.