e-CRF
Electronic CRF for investigators
Electronic CRF (e-CRF: Electronic Case Report Form data entry) allows every investigator to collect online data and to participate in therapeutic and epidemiology clinical trials. It helps investigators include their patients, and when required, allocate them to the right randomization arm generated automatically by the database. Electronic CRF allows every investigator to follow the status of each patient online. Furthermore the quality of the data can be checked at the time of data capture. Each investigator has the right to manage their study process to check its evolution daily and modify the information if needed. Access is provided to the full audit trail history of modifications for improved follow-up of patient data.
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