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RCR Forum: What Makes a Good Informed Consent Process?

Tuesday, March 7, 2017
3:00 pm to 5:00 pm

Holly Williams
Associate Director, Campus Human Subjects Protections Program

In this forum, staff from the Institutional Review Board for Protecting Human Subjects in Non-Medical Research (IRB) will discuss consent protocols and waivers, and will be of interest to students in any graduate program who expect to be conducting social/ behavioral science research involving human subjects. In the workshop, you will engage in and exercises for developing comprehensible, participant-friendly processes for ensuring fully-informed human research subjects.
 

Location

French Family Science Center 2231 (Bonk Auditorium)
Map

Event Category

  • Professional Development