The case report form (CRF) is the primary data collection tool in clinical trial conduct, analysis, and reporting of results. The sponsor is responsible for development of a CRF that accurately represents the protocol, management of CRF production, monitoring, and auditing. The study site is responsible for accurate and timely completion of the CRF. This short course provides an overview of key elements in design and management of the CRF.
|Dates||Days and Times||Location||Faculty|
Course fee: $210
To access the online class, visit http://ilearn.sfsu.edu to log in after registration and payment using SF State ID and password.
|Refund Code||Full Refund||75% Refund||No Refund|
|CEL_1SUM||Class dropped one day prior to class start day||N/A||Class dropped on or beyond class start day|
Last Update: Jul 14, 2020 1:30pm