Current clinical trial methods for collecting, managing and monitoring site data are inefficient, outdated and cumbersome. By leveraging direct data capture technologies, sponsors can reduce monitoring and data management costs by 30% or more.
In this webinar, the speakers discuss the benefits of moving from the traditional industry model to a Central eSource model in which sites capture data electronically as source, which then becomes the electronic care report form (eCRF). This direct data capture (DDC) model eliminates the need for sites to transcribe data into a secondary EDC and for Clinical Research Associates (CRAs) to perform most forms of source data verification – enabling a more agile, risk-based monitoring approach where data review can occur closer to data collection. Moreover, by centralizing and remote-enabling the monitoring, the DDC model improves the CRA’s productivity and retention.
See for yourself how the technology’s cost is only a small portion of the overall study budget — but the operational efficiencies that it enables are where real savings accrue.
The solution that reduces monitoring costs and increases data quality is clearly CRIO.