Drugs, biologics, and devices require structured clinical testing in humans prior to approval for marketing and post-marketing safety surveillance. This class provides an introduction to the clinical research industry including trends and opportunities, clinical program and trial development and management, regulations, ethics, and the role of regulatory agencies, sponsors, investigators, IRBs, and the public as study subjects or patients.
|Dates||Days and Times||Location||Faculty|
|1/28/20-3/3/20||Tues, 6:00PM-7:30PM||Online||Tenea Nelson|
Course fee: $495
|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: Feb 14, 2020 9:37am