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Checklists

HRP-401 – CHECKLIST Pre-Review

HRP-402 – CHECKLIST Non-Committee Review

HRP-410 – CHECKLIST Waiver or Alteration of Consent Process

HRP-411 – CHECKLIST Waiver of Written Documentation of Consent

HRP-412 – CHECKLIST Pregnant Women

HRP-413 – CHECKLIST Non-Viable Neonates

HRP-414 – CHECKLIST Neonates of Uncertain Viability

HRP-415 – CHECKLIST Prisoners

HRP-416 – CHECKLIST Children

HRP-417 – CHECKLIST Cognitively Impaired Adults

HRP-418 – CHECKLIST Non-Significant Risk Device

HRP-419 – CHECKLIST Waiver Consent Process – Emergency Research

HRP-427 – CHECKLIST Post Approval Monitoring: Drug or Device Clinical Trial

HRP-428 – CHECKLIST Post Approval Monitoring: Participant File

HRP-429 – CHECKLIST Post Approval Monitoring: Biomedical Research

HRP-430 – CHECKLIST Post Approval Monitoring: Social Behavioral Research

HRP-431 – CHECKLIST Minutes – Quality Improvement Assessment

HRP-432 – CHECKLIST Quality Assurance Assessment

HRP-441 – CHECKLIST HIPAA – Waiver Authorization

HRP-442 – CHECKLIST Genetic Biobanking Studies

HRP-443 – CHECKLIST Observation of the Consent Process

HRP-1401 – CHECKLIST Post Approval Monitoring: Recruitment Activities

HRP-1403 – CHECKLIST IRB Member Appointment

HRP-1404 – CHECKLIST IRB Member Re-Appointment

HRP-1405 – CHECKLIST Post Approval Monitoring: Registry, Data Review, and/or Specimen Collection

HRP-1406 – CHECKLIST Post Approval Monitoring: Studies Under External IRB Review

HRP-1407 – CHECKLIST Post Approval Monitoring: Site File

HRP-1408 – CHECKLIST Principal Investigator (PI) Transfer of Responsibilities