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 or 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)My IRB ContactToolkit Expand Toolkit section SOPsChecklistsWorksheetsTemplatesSubmitting to the IRB Expand Submitting to the IRB section Before you submitHow to SubmitAfter you submitAfter ApprovalRequired Trainings Expand Required Trainings section Human Subject Protection Training in CITITrainTraq TrainingHuman Subjects Research DeterminationReporting to the IRBNews and UpdatesFAQParticipant 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 FormResearch Compliance and Biosafety
