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A Case Report Form (CRF) is an electronic or paper document which is used in a clinical trial to record the protocol and required information about each participant. It enables efficient and complete data collection, processing, analysis and reporting.
A Case Report Form, or CRF, is a research-specific document that collects all the relevant data for a given protocol. Historically, these were completed on paper but for most current studies, data is reported into an Electronic Data Capture database (or EDC).
Designed to intuitively track and logically structure information, CTMS enables life science teams to monitor and report on clinical trial progress and make better informed decisions, providing the best quality data while ensuring patient safety.
Case reports should encompass the following five sections: an abstract, an introduction with a literature review, a description of the case report, a discussion that includes a detailed explanation of the literature review, and a brief summary of the case and a conclusion.
A case report form (CRF) is a document designed to record all patient information that needs to be collected during a clinical trial. An electronic CRF (eCRF) can be stored in cloud-based systems such as clinical metadata repositories (CMDRs) or Electronic Data Capture (EDC) systems.
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The size of a CRF can range from a handwritten one-time snapshot of a patients physical condition to hundreds of pages of electronically captured data obtained over a period of weeks or months. (It can also include required check-up visits months after the patients treatment has stopped.)
Case reports generally take the format of: Background. Case presentation. Observations and investigation. Diagnosis. Treatment. Outcome. Discussion.

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