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These two types of CRFs are referred to as single-section and multi-section CRFs, respectively. No matter how many sections comprise a CRF, you view and work on one section at a time.
A case report form (or CRF) is a paper or electronic questionnaire specifically used in clinical trial research. The case report form is the tool used by the sponsor of the clinical trial to collect data from each participating patient.
A case report form (or CRF) is a paper or electronic questionnaire specifically used in clinical trial research. The case report form is the tool used by the sponsor of the clinical trial to collect data from each participating patient.
Rather than paper CRFs, collecting clinical data in a digital format with an eCRF means that the data can be securely uploaded to the cloud and shared with other stakeholders in near-real time. Furthermore, a well-developed EDC system will allow for more accurate and easier data entry.
These two types of CRFs are referred to as single-section and multi-section CRFs, respectively. No matter how many sections comprise a CRF, you view and work on one section at a time.
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Primary objective of CRF designing is to gather complete and accurate data by avoiding duplication and facilitating transcription of data from source documents onto the CRF. CRF should be designed with the primary safety and efficacy endpoints as the main goal of data collection.
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.
Case Report Form (CRF) ▪ A printed, optical or electronic document designed to record all of the. protocol-required information to be reported to the sponsor on each trial. subject (ICH E6 GCP Guidelines) ▪ An informative and well-structured CRF simplifies database design.

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