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Contact Information
| Contact Information for Research Integrity Office | |
|---|---|
| Phone | (775) 327-2368 |
| Fax | (775) 327-2369 |
| Location |
Ross Hall
Room 218/Mail Stop 0331 |
| Address | 1664 N. Virginia Street Reno, NV 89557-0331 |
| Contact | Contact the Office |
IRB Member and Reviewer Info
Information for IRB Members
- Human Research Protection Policy Manual
- Belmont Report
- Title 45 CFR Part 46
- Expedited Review Categories
- Title 21 CFR Part 50
- Title 21 CFR Part 56
Research Resources
- Site-specific Research Procedures
- Training
- OHRP Educational Videos
- OHRP IRB Guidebook
- Completing a First-rate Review: Your Responsibilities as an IRB Reviewer: PPT/PDF
- Data Safety Monitoring Plans (DSMP): PPT/PDF
Reviewer Checklists
- I7 CH1 Review of Research Involving Investigational Drugs or Devices
- II2 CH1 Review of Exempt Research
- II2 CH2 Review of New Protocol
- II2 CH3 Review of Expedited Categories
- II2 CH4 Review of Renewals and Amendments
- II2 CH5 Review of Renewal, Expedited Category 8(a)
- II2 CH6 Review of Renewal, Expedited Category 8(b)
- II2 CH7 Review of Renewal, Expedited Category 8(c)
- II3F CH1 Review of Consent and HIPAA Authorization Waivers
- II4A-B CH Review of Research Involving Pregnant Women, Human Fetuses and Neonates
- II4A-C CH Review of Research Involving Prisoners
- II4A-D CH Review of Research Involving Children
Reviewer Checklists for Assessing Agency-specific Requirements
- I1D CH4 Review of Research Involving the Department of Defense
- I1D CH5 Review of Research Involving the Department of Education
- I1D CH6 Review of Research Involving the Environmental Protection Agency
IRB Member Factsheets
IRB Member Factsheets are provided to assist members with their research and to help illustrate the various aspects of quality institutional review board procedures.
- Belmont Report Info
- Brief Overview of Regulatory Basis of IRB Authority
- Children: Regulations
- Continuing Review & Changes of Protocol
- Criteria for IRB Approval
- Drugs, Biologics, and Devices
- Informed Consent Process
- Investigator Conflicts of Interest
- IRB Member Conflicts of Interest
- IRB Responsibilities Related to Review of VA Research
- Noncompliance, Protocol Exceptions and Deviations
- Overview of the Accreditation Process
- Pregnant Women, Fetuses and Neonates
- Prisoner Regulations
- Privacy & Confidentiality
- Review Processes
- Unanticipated Problems
