eSource DDC

The general term “eSource DDC” refers to an electronic application and/or device that allows direct entry of source data, and to directly identify some of these data as CRF (Case Report Form) data, for clinical trial purposes at the point of care by investigator site staff, for example via an electronic tablet (Source – EMA Qualification Opinion on eSource Direct Data Capture (DDC), July 2019 (EMA/CHMP/SAWP/483349/2019)).

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