Regulatory authorities may conduct routine or for-cause inspections of sponsor and study sites during clinical trials and routine inspections prior to product approval. This is an overview of FDA and sponsor audit procedures, roles, processes, and responses to findings.
|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_1||Class dropped one day prior to class start day||N/A||Class dropped on or beyond class start day|
Last Update: Jul 06, 2020 7:49pm