A case report form (or CRF) is a paper or electronic questionnaire specifically used in clinical trial research. [1] The case report form is the tool used by the sponsor of the clinical trial to collect data from each participating patient.

Case report form (CRF) is a specialized document in clinical research. It should be study protocol driven, robust in content and have material to collect the study specific data.

Our free, downloadable CRF design checklist can help you design quality case report forms that meet all your study requirements.

What are case report forms? 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.

Mar 3, 2020 · A CRF is a set of documents that collects data and information from a clinical trial. The CRF is used by the study sponsor to capture and retain important data in the clinical trial. CRFs are usually electronic but may also be created in paper form.

A CRF is a document that is used to compile all protocol-related information for each participant in a clinical trial. This data can include everything from participants’ personal information to study visit results to treatment outcomes and side effects experienced.

Jan 6, 2024 · A Case Report Form (CRF), is 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, as defined by the International Conference on Harmonization Guidelines for …

Case report forms (CRFs) are critical documents in clinical research that record study data for each participant. Careful design of CRFs is crucial for capturing complete, accurate, reliable data that can withstand scientific and regulatory scrutiny.

When you define a CRF for use in OpenClinica, you use Excel (1997 to 2003 version) to provide the content in these four tabs (sheets) of the CRF .xls file: CRF; Sections; Groups; Items; Each tab contains column headers that specify what belongs …

CRF creation can begin as soon as the final study protocol is available. The final protocol should specify all required data items. The CRF should be finalised prior to enrolling participants. It is advisable to develop the CRF in conjunction with the database, which will be used for data analysis. How to develop the CRF