Huron IRB - Toolkit Document Crosswalk
Estimated Reading Time: 6 MinutesWith the implementation of the Huron IRB system, the existing Ohio State Human Research Protection Program (HRPP) policies have been retired and replaced with Huron toolkit documents. The schema below will provide a crosswalk to assist in navigating where the Ohio State information transferred into the Huron documents. All resources to support the IRB submission process can be found in the "Library" tab in the Huron IRB system.
HRPP Policy |
SOP |
Investigator Manual |
Worksheet |
Checklist |
Other |
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Human Research Protection Program (these policies remain unchanged) |
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Research Involving Human Subjects |
ORRP Webpages |
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Organizational Financial Conflicts of Interest |
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Noncompliance |
HRP-026-Suspension or Termination Issued Outside of a Convened IRB |
HRP-103 | HRP-321-Review of Information Items | ||
Responsibilities of Principal Investigators, Co-Investigators, and Key Personnel |
HRP-103 | ||||
HRPP Policies and Procedures |
HRP-505-Template SOP |
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HRPP Quality Improvement Activities |
HRP-431-Minutes Quality Improvement Assessment |
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Exempt Research |
HRP-103 | ||||
Submission and Pre-Review |
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Board and Reviewer Assignment for Convened Review |
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Review of Research by the Convened IRB |
HRP-103 |
HRP-310-Human Research Determination HRP-311-Engagement Determination HRP-317-Short Form of Consent Documentation HRP-318-Additional Federal Agency Criteria |
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IRB Actions and Communications |
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Expedited and Administrative Review Procedures |
HRP-103 | ||||
Suspension and Termination of IRB-Approved Research |
HRP-026-Suspension or Termination Issued Outside of a Convened IRB |
HRP-103 | |||
Recruiting Methods, Recruitment Materials, and Participant Compensation |
HRP-103 | ||||
Privacy and Confidentiality |
HRP-103 |
HRP-410-Waiver or Alteration of Consent Process |
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Informed Consent Process and the Elements of Informed Consent |
HRP-103 | HRP-314-Criteria for Approval | |||
Documentation of the Informed Consent Process |
HRP-103 | HRP-411-Waiver of Written Documentation of Consent | |||
Assent and Parental Permission |
HRP-103 |
HRP-416b-Checkist-Waiver of Parental Permission |
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Short Form Informed Consent |
HRP-090-Informed Consent Process for research | HRP-103 | HRP-317-Short Form of Consent Documentation | ||
Data Safety and Monitoring |
HRP-103 | ||||
Event Reporting |
HRP-025-Investigations HRP-026-Suspension or Termination Issued Outside of a Convened IRB |
HRP-103 | HRP-321-Review of Information Items |
HRP-214-Reportable New Information HRP-216-RNI Supplement |
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Research Involving Pregnant Women, Fetuses, or Neonates |
HRP-030-Designated Reviewers | HRP-103 | HRP-314-Criteria for Approval |
HRP-414-Neonates of Uncertain Viability
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Research Involving Prisoners |
HRP-030-Designated Reviewers | HRP-103 | |||
Research Involving Children |
HRP-103 | HRP-314-Criteria for Approval | |||
Vulnerable Populations |
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Research Involving Investigational Drugs |
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Research Involving Medical Devices |
HRP-030-Designated Reviewers | ||||
Research Involving Data and/or Biological Specimens (These policies remain unchanged.) |
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Planned Emergency Research |
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Emergency Use of Investigational Drugs, Biologics, or Devices |
HRP-023-Emergency Use, Compassionate Use, Indvidual Patient Expanded Access |
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IRB Composition and IRB Member Roles and Responsibilities |
HRP-501-Meeting Minutes HRP-601-Database |
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IRB Member and Consultant Conflict of Interest |
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IRB Reporting |
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IRB Recordkeeping |
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Collaborative and Multi-Site Research |
HRP-801-Establishing Authorization Agreements HRP-802-Institutional Profile Management |
ORRP Webpage |
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Research Involving Radiation |
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Additional Requirements for Clinical Research: ICH-GCP |
HRP-001-Definitions | HRP-103 | |||
Additional Requirements for Research Sponsored by DOD |
HRP-001-Definitions | HRP-103 | |||
Additional Human Subjects Protection Requirements Based on Federal Agency Funding |
HRP-013-LAR's, Children, and Guardians | HRP-103 |
Please note that as Ohio State transitions from Buck-IRB to Huron IRB for human subjects research submission, review and approval, some aspects of the Human Research Protection Program (HRPP) website may be outdated. Revisions are in progress; however, if you are unable to find the information you are looking for, please contact IRBinfo@osu.edu for assistance.