Case report Forms (CRFs) are standardized documents in which the study team records data collected in a clinical trial.  CRFs should support compliant collection and documentation of research data by following Good Clinical Practice and Good Documentation guidelines.  This seminar will cover definitions, operational considerations, and data requirements, while focusing on data outputs (data analysis, IRB/FDA/DSMB reporting, repository storage) to inform the content and form (paper/electronic) of your CRFs.