SOP's | Human Subject Research Office

Standard Operating Procedures followed by the human research protection program at the University of Miami

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Standard Operating Procedures

HRP-001 - SOP - Definitions

HRP-012 - SOP - Observation of Consent Process

HRP-013 - SOP - LARs, Children, and Guardians

HRP-020 - SOP - Incoming Items

HRP-021 - SOP - Pre-Review

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-051 - SOP - Consultation

HRP-052 - SOP - Post-Review

HRP-060 - SOP - Annual Evaluations of the HRPP

HRP-061 - SOP - Monthly Evaluations of the HRPP

HRP-062 - SOP - Daily Tasks

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-070 - SOP - IRB Records

HRP-071 - SOP - Standard Operating Procedures

HRP-072 - SOP - IRB Records Retention

HRP-080 - SOP - IRB Formation and Registration

HRP-081 - SOP - IRB Removal

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-097 - SOP - COI Review

HRP-801 - SOP - Establishing Authorization Agreements

HRP-802 - SOP - Institutional Profile Management

HRP-803 - SOP - Reliance Pre-Review

HRP-804 - SOP - External IRB Post-Review

HRP-805 - SOP - External IRB Updates

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