IRB Resources and Guidance

• HIPAA & Human Subjects Research

• General Data Protection Regulation (GDPR)

• Exempt Review Categories

• Expedited Review Categories

• Reasons for IRB application delays

• Minimal Risk Tip Sheet

• Informed Consent Guide

• Guidance - Online Survey Research and Bots

• Guideline - Field Experiments and Elections

• Incidental Findings Guide

• Guidance - Significant Risk (SR) & Non-significant Risk (NSR) devices

• Best practices for doing research with participants remotely

• Attending Zoom Meetings

(more document links will be added soon)

• IRB002 Institutional Review Board (IRB) Applicability and Authority
• IRB003 IRB Membership
• IRB004 IRB Review Process
• IRB005 Convened IRB Meeting Administration
• IRB006 IRB Records
• IRB007 Evaluation of IRB Operations
• IRB008 Principal Investigator Responsibilities
• IRB009 Unanticipated Problems
• IRB010 Non-Compliance and Reporting
• IRB011 Research Involving Vulnerable Populations
• IRB012 Student Research
• IRB013 Deception
• IRB014 International Research
• IRB015 Oral History
• IRB016 Reliance Agreements and Multiple Site Studies
• IRB017 Financial Conflict of Interest
• IRB018 Research Involving HIPAA
• IRB019 Certificate of Confidentiality
• IRB020 Genetic Studies
• IRB021 Research Involving Coded Private Information or Biological Specimens
• IRB022 Review of Devices
• IRB023 Agency-Specific Regulations
• IRB024 IRB Glossary – Abbreviations and Definitions
• Policy – Use of Subject Pools in Human Subjects Research

• NIH Genomic Data Sharing (GDS) Policy and the Genome-Wide Association
  Studies (GWAS)

   

Previous SOPPs (For Reference Only)

• IRB001 Institutional Review Board (IRB) Standard Operating Policies and
  Procedures
• 2019 Addendum for the Revised Common Rule

• UCR Researchers: Collaborative Institutional Training Initiative (CITI) Instructions

• Non-UCR Collaborators: CIRTification Training for Community Members/Partners

• IRB Office Hours

• 45 CFR 46 (Human Subjects)

• CFR 21 (Food and Drugs)

• The Belmont Report

• NIH - Research Involving Human Subjects

• ClinicalTrials.gov Registry

• NIH - Glossary of Human Subjects Terms

• International Compilation of Human Research Standards

• IRB Member Reviewer Checklist

• IRB Member Placemat

• 'How to IRB' tutorial (optimized for Chrome)

• Exempt Review Categories - for pre-2019 Applications