Resources

Found 16 Items.

Content Type	Title
Office	Institutional Review Board for Human Participant Research (IRB) Office
News	Single IRB (sIRB) Regulatory Requirements in Effect January 20, 2020
Contact	Joyel Moeller - Senior IRB Administrator and Reliance Specialist
Process	Research with Human Participants
Resource	About the IRB Committee
Resource	The Life Cycle of an IRB Protocol
Resource	IRB Announcements & Newsletters
Resource	IRB Informed Consent
Resource	IRB Training
Resource	IRB Considerations: Human Participant Data, Data Sets and Internet Research
Resource	IRB Biomedical Research
Resource	IRB Considerations for International Research
Resource	IRB Considerations for Clinical Trials
Resource	Report a Concern Involving Human Participant Research
Resource	IRB FAQs
Resource	IRB Guidance and Resources