“Informed Consent 101” will review expectations for obtaining consent from participants in biomedical and social-behavioral research. Content will include required elements of consent, HIPAA authorization, tips for making consent a […]
“eIRB 101” will provide a technical overview of how to use the IRB’s new submission system, eIRB. This session will review how to access eIRB, submit various types of applications, […]
“How to Submit Initial Protocols” will cover everything you need to know about submitting a new initial application for IRB review. This session will focus on the substance of an […]