New to the IRB
- IRB Members Guide
- Acronyms
- CITI Training
- Educational Offerings
- Ethical Guidelines
- Glossary
- IRB-HSR Administrative Staff
- Meeting Dates
- Federal Government Human Research Protection Org Chart
- IRB Member IRB Chair Approval Criteria Checklist
- Continuations Checklist Full Board
- Device Risk Determination SR vs. NSR Checklist
- Full Board Modification Scientist Reviewer Checklist
- Full Board Modification Non Scientist Reviewer Checklist
- HUD_Reviewers Checklist
- HUD Continuing Reviewer Checklist
- Investigational Drug Service Review Checklist- Modifications
- Investigational Drug Service Review Checklist- New Protocol
- IRB Member Expedited Event or Condition Response 2018 Common Rule Checklist
- IRB Member Event or Condition Response Pre-2018 Common Rule
- IRB Member Scientific Reviewer Checklist - New Study
- Non-Scientist Reviewers Checklist 2018 Common Rule
- Retention Incentives Checklist
- Protocol Deviation Review Checklist
- Scientific Reviewer Checklist-Planned Emergency Research and EFIC
- Serious Adverse Event/Unanticipated Problem Review Checklist
- Statistical Review Checklist
- Vulnerable Populations Checklists
Federal Regulations and Other Useful Resources
- Federal Wide Assurance (FWA)
- Federal Regulations
- Resources for International Research
- Useful Websites and Links
Other IRB References
- Hastings Center - Ethics and Human Research Publication
- HHS/OHRP - IRB Guidebook
- FDA - Guidance for IRBs
- PRIM&R Public Responsibility in Medicine and Research, otherwise known as PRIM&R, is a non-profit organization for those committed to promoting the highest ethical standards in the conduct of research. PRIM&R develops educational programs for those charged with the review and conduct of research.
- IRB Forum Member web site and e-mail list to promote the discussion of ethical, regulatory and policy concerns with human subjects research. E-mail list messages can be received in a combined digest format.