HRP-012 - SOP - Observation of Consent Process HRP-013 - SOP - LARs, Children, and Guardians HRP-020 - SOP - Incoming Items HRP-023 - SOP - Emergency Use, Compassionate Use, & Patient Expanded Access Review HRP-024 - SOP - New Information HRP-026- SOP - Suspension or Terminations Outside of Convened IRB HRP-030 - SOP - Designated Reviewers HRP-031- SOP - Non-Committee Review Preparation HRP-032 - SOP - Non-Committee Review Conduct HRP-040 - SOP -IRB Meeting Preparation HRP-041 - SOP - IRB Meeting Conduct HRP-042 - SOP - IRB Meeting Attendance Monitoring HRP-043 - SOP - IRB Meeting Minutes HRP-044 - SOP - Not Otherwise Approvable Research HRP-050 - SOP - Conflicting Interests of IRB Members HRP-060 - SOP - Annual Evaluations of the HRPP HRP-061 - SOP - Monthly Evaluations of the HRPP HRP-063 - SOP - Expiration of IRB Approval HRP-064 - SOP - NIH GDS Institutional Certification HRP-065 - SOP - Response Plan for Emergencies-Disasters Impacting the HRPP HRP-071 - SOP - Standard Operating Procedures HRP-072 - SOP - IRB Records Retention HRP-080 - SOP - IRB Formation and Registration HRP-082 - SOP - IRB Membership Addition HRP-083 - SOP - IRB Membership Removal HRP-084 - SOP - IRB Meeting Scheduling and Notification HRP-090 - SOP - Informed Consent Process for Research HRP-091 - SOP - Written Documentation of Consent HRP-092 - SOP - COVID-19 Risk Mitigation Planning HRP-801 - SOP - Establishing Authorization Agreements HRP-802 - SOP - Institutional Profile Management HRP-803 - SOP - Reliance Pre-Review
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