Planning on doing research with human subjects, but not sure where to start? Attend this informational session and we'll give you all the information you need to start writing a human research protocol that can make it through the IRB review process quickly and easily. Topics covered include the different review categories, required elements of a protocol, required elements of an informed consent document, and how to make a protocol amendment after approval is obtained.
IRB Basics informational session
Monday, August 21, 2017 9:00am - 10:00am