Central eSource: How Sponsors Can Leverage Site Technology To Standardize Quality And Improve Site Performance

In this webinar, CRIO founder and co-CEO Raymond Nomizu explores how clinical trial sponsors can capitalize on the growing adoption of electronic source (eSource) technology at research sites. The focus is on Central eSource, a powerful approach that enables sponsors to create standardized electronic source templates that are pre-mapped to the electronic case report form (eCRF). These templates are then sent to sites, which can customize them according to their standard operating procedures (SOPs).

This method offers multiple advantages, as it streamlines site startup, enhances data quality at the point of capture, reduces time to Electronic Data Capture (EDC) entry, and enables effective centralized remote monitoring. Attendees will gain key insights into the current landscape of source data collection and storage at clinical trial sites,  the crucial distinctions between eSource and electronic data capture (EDC), and the definition and benefits of Central eSource compared to traditional data collection approaches. Don’t miss the opportunity to stay ahead of the curve and transform your clinical data strategy.