Modernizing electronic data capture (EDC) is critical for conducting more effective clinical trials. From improving the accuracy of electronic case report forms (eCRFs) to streamlining the entire site experience, running high-quality studies requires exceptional clinical trial data management. At a recent Veeva Summit on R&D and Quality, Jill Janssen, director of Vanderbilt University Medical Center and Alesia Pruitt, research coordinator at Vanderbilt Clinical Trials Center, discussed how EDC systems impact their study start-up and training, data entry quality, operational reporting, and more. Accelerating clinical trials by bringing together study start-up activities.

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