DIA 2023

Today, sponsors require already overburdened research sites to use their systems and technology. By harnessing site collected eSource data, sponsors and CROs can benefit from streamlining clinical trial operations and improving patient safety. Further, with eSource technology, CRAs can carry out centralized, remote clinical data review and monitoring which frees up their time on site, to focus on patients and the critical aspects of clinical trial oversight. The greatest benefit of eSource technology is the ability to access study data in real-time. Reducing the monitoring review timelines is essential for early risk and issue detection. Resolving issues in real-time enables corrective action for all patients, not just preventative action for future patients.

Key Takeaways:

At the end of this Innovation Theater presentation, attendees will have a better understanding of:
– How eSource allows for better clinical data
– What continuous monitoring is and how it’s used

– How continuous remote monitoring improves patient safety