Policies and Procedures
Institutional Review Board (IRB) at Nationwide Children's Hospital Standard Operating Procedure (SOP) Documents
- HRP-001 - Definitions
- HRP-012 - Observation of Consent Process
- HRP-013 - LARs, Children, and Guardians
- HRP-020 - Incoming Items
- HRP-021 - Pre-Review
- HRP-022 - Humanitarian-Use-Devices
- HRP-023 - Emergency Use, Compassionate Use, Indiv Patient Expanded Access
- HRP-024 - New Information
- HRP-025 - Investigations
- HRP-026 - Suspension or Termination
- HRP-027 - Emergency Use, Comp. Use, Individual Patient Access Post Review
- HRP-030 - Designated Reviewers
- HRP-031 - Non-Committee Review Preparation
- HRP-032 - Non-Committee Review Conduct PRE-2018
- HRP-040 - IRB Meeting Preparation
- HRP-041 - IRB Meeting Conduct
- HRP-042 - IRB Meeting Attendance Monitoring
- HRP-043 - IRB Meeting Minutes
- HRP-044 - Not Otherwise Approvable Research
- HRP-050 - Conflicting Interests of IRB Members
- HRP-051 - Consultation
- HRP-052 - Post-Review
- HRP-054 - Institutional Conflicts of Interests
- HRP-055 - Research Conflict of Interest
- HRP-060 - Annual Evaluations of the HRPP
- HRP-061 - Monthly Evaluations of the HRPP
- HRP-063 - Expiration of IRB Approval
- HRP-064 - NIH GDS Institutional Certification
- HRP-065 - Response Plan for Emergencies-Disasters Impacting the HRPP
- HRP-070 - IRB Records
- HRP-071 - Standard Operating Procedures
- HRP-072 - IRB Records Retention
- HRP-080 - IRB Formation and Registration
- HRP-081 - IRB Removal
- HRP-082 - IRB Membership Addition
- HRP-083 - IRB Membership Removal
- HRP-084 - IRB Meeting Scheduling and Notification
- HRP-090 - Informed Consent Process for Research
- HRP-091 - Written Documentation of Consent
- HRP-103 - NCH Investigator Manual
- HRP-601 - IRB Roster
- HRP-801 - Establishing Authorization Agreements
- HRP-802 - Institutional Profile Management
- HRP-803 - Reliance Pre-Review (formerly Site Validation)
- HRP-804 - External IRB Post-Review (formerly Site Pre-Review)