Case Report Form
The CCTS Regulatory Support and Advocacy Core collaborated with members of the Office of the Vice Chancellor for Research's (OVCR) Quality Improvement Program to develop a set of standard case report forms that are now available on the OVCR website. The forms should be useful for any investigator initiated clinical trials and can be customized to an individual study.
A Case report form (CRF) is a printed, optical, or electronic document designed to record all protocol-required information on each subject in a clinical research study. The CRF facilitates complete and standardized data collection that promotes efficient processing, analysis, and reporting of information, as well as exchange of data across sites and to the Sponsor/Principal Investigator/Data Coordinating Center.