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|
|10/19/19-10/26/19||Sat, 10:00AM-1:00PM||Online||Thomas Tremblay|
Course fee: $210
|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: Oct 15, 2019 8:36am