eSource has the potential to change the antiquated process of capturing data during a clinical trial.
TORONTO (PRWEB) July 29, 2020
eSource has long been touted as the solution to high data management and monitoring costs and inefficiencies. This webinar will cover the history of eSource, the reasons it did not take off as quickly as people initially expected, and where eSource is headed. From EMR/EHR to wearables, to site source, the industry is moving towards capturing data electronically for clinical trials and then repurposing it for downstream analysis, at a far higher volume than usual due to COVID-19.
eSource has the potential to change the antiquated process of capturing data during a clinical trial. The effect on the efficiency of monitoring, site and data management processes is significant. Join this webinar to hear first-hand how one CRO leveraged eSource to lower overall costs for sites, data management and monitoring.
This webinar will provide a grounding in what eSource is, how it can be deployed, the practical implementation of eSource and how to avoid hurdles in the process.
Join Stephen Boccardo, SVP Business Development, and Commercial Strategy, Quartesian and Lisa Charlton, PhD, MBA, Product Manager of Participant Engagement, ePro and eConsent, Medrio in a live webinar on Tuesday, August 18, 2020 at 10am EDT (3pm BST/UK).
For more information or to register for this event, visit eSource: A Piece of the Virtual Trial Puzzle.
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