Detroit, MI 48201
IRB Training Sessions are open to all students, faculty and affiliated staff interested in learning about IRB review of research.
An overview of the IRB submission requirements will be presented for FDA regulated projects involving investigational drugs, biologics, and devices. In addition, information will be provided on single time emergency use of drugs and devices, treatment use of drugs and devices, and special requirements for humanitarian use devices.
When: Tuesday, August 19, 2014, 1:00 pm – 2:00 pm
Where: WSU Medical Campus, Scott Hall, Room 1140
Speaker: Ray-Nitra Pugh, Education Coordinator, IRB Administration Office