Checklists HRP-401 Pre-Review HRP-402 Non-Committee Review HRP-405 Limited IRB Review HRP-410 Waiver of Alteration of Consent Process HRP-411 Waiver of Written Documentation of Consent HRP-412 Pregnant Women HRP-415 Prisoners HRP-416 Children HRP-417 Cognitively Impaired Adults HRP-418 Non-Significant Risk Device HRP-441 HIPAA Waiver of Authorization Human Research Protection Program (HRPP)Research Compliance and BiosafetyWhat is the Human Research Protection Program (HRPP)?IRB Hot TopicsApproval Process Expand Approval Process section Is it Human Subject Research?What to submit?How to Submit an Application?What happens to my application once submitted?What happens after approval?My IRB ContactToolkit Expand Toolkit section SOPsChecklistsWorksheetsTemplatesRequired Trainings Expand Required Trainings section Human Subject Protection Training in CITITrainTraq TrainingNews and UpdatesInvestigator ResourcesFAQParticipant InformationIRB Meeting InfoUniversity Rule on Human Subjects in ResearchRevised Common RuleOther Resources Expand Other Resources section Tips for Writing Consent FormsQuality Assurance/Post Approval Monitoring ProgramAAHRPP Accreditation InformationPayments to Human Research ParticipantsHuman Subjects Concern Submission Form