case report form


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case report form

EBM
(1) A printed, optical or electronic document designed to record all of the protocol-required information to be reported to the sponsor for each subject/patient in a clinical trial.
(2) A record of clinical study observations and other information that must be completed for each subject in a clinical trial, per study protocol mandate. CRF can refer to either a CRF page (which contains one or more data items linked together for collection and display) or a casebook (which includes all CRF pages on which a set of clinical study observations and other information can be or have been collected, or the information collected by completion of such CRF pages for a subject/patient in a clinical study).
References in periodicals archive ?
As a result, health officials in King County have developed a case report form to try to triage the more intensive partner notification services, such as the use of disease intervention specialists.
Also, there may have been sex differences in health insurance status and other predictors of mortality that were not recorded on the case report form.
Education is the third major benefit of the case report forms.
Once you begin to conduct several studies, hire a lab technician or research coordinator who can be responsible for the budget, consent forms, and case report forms.
A case report form (or CRF) is a paper or electronic questionnaire (ECRF if electronic) used in clinical trial research.
CompleClinical captures electronic patient reported outcomes (ePRO) data, also known as diary data, electronic case report form (eCRF) data, and physiological data (such as electrocardiograms [ECG], vital signs, spirometry, radiological images, and laboratory results).
Attendees will learn how making the monitoring function more efficient improves the quality of the site visit; how the reporting tools in EDC systems make it easier to see the status of the trial from multiple perspectives; and how to attach images to the Case Report Form to boost the value of the CRF contents.
DUBLIN, August 11 /PRNewswire-FirstCall/ -- ICON plc (NASDAQ: ICLR; ISIN:IE0005711209), a global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries, today announced that its Medical Imaging division has become the first commercial imaging core laboratory to offer Quantitative Coronary Angiographic (QCA) analysis with an integrated electronic Case Report Form (eCRF).
500, supports clinical trial data collection and management with innovative technology solutions including Electronic Data Capture with specialized Clinical Data Management services, IWRS (web-based patient randomization and drug/device supply management), Clinical Trial Management Systems and digital on-demand Case Report Form publishing management software.
Value-added SharePoint web parts to assist with reporting study enrollment, subject completion, Case Report Form (CRF) progress, and clinical site payment tracking are also planned for the upcoming release.
0 release include: greatly expanding the bi-directional updates for information exchange between OSCTM and Microsoft Office SharePoint Server (MOSS) through use of ClinBUS([R]), TranSenda's advanced data interchange technology; the ability to create Microsoft's InfoPath forms and bind them to SharePoint lists, making the process of data collection and review much easier; capability to create ad-hoc events and case report form (CRF) pages, resulting in sleeker and deeper integration with electronic data capture applications; enhanced connectivity between global configuration settings and study-specific parameters; and ease-of-use improvements such as expanded identifier variables, advanced address handling and dedicated sign-in assistance.