The FDA and other regulatory agencies establish rules and guidelines for clinical development and marketing of medical products. This course provides an overview of the regulatory pathway necessary to gain approval to market medical products. Upon completion of this course, you will have a basic understanding of the regulations involved in clinical development and understand how manufacturing and preclinical/nonclinical areas interact with clinical development.
|Dates||Days and Times||Location||Faculty|
|11/16/20-12/7/20||Mon, 6:00PM-7:30PM||Online||Ronald Lillie|
Course fee: $310
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