Electronic Source (eSource) and Electronic Data Capture (EDC) are increasingly popular technologies for collecting and managing clinical trial data. The two types of systems are less similar than their names suggest.
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What is eSource? According to the FDA, eSource is defined as “data initially recorded in electronic format. They can include information in original records and certified copies of original records of clinical findings, observations, or other activities captured prior to or during a clinical investigation used for reconstructing and evaluating the investigation.” eSource is already...
In order to increase diversity in clinical trials, it is important to include voices from many different communities and roles. For this blog post, CRIO employee Stefanie Palmer sat down for a discussion with Dr. Hadi Danawi to talk about involving the Arab American community and people from Middle Eastern backgrounds in clinical research. Who...
Over 70% of clinical trial data today comes from non-case report form data. Non-case report form data includes continuous data such as wearable data, lab data, patient reported data and ECG data, to name a few. Generally speaking, these are all collected as source without transcription or entry into another system. Today, we have reached...
