IRB New Member Training
This comprehensive overview of the role and responsibilities of IRB members is required for all new members. It can also be completed as a refresher for active IRB members.
Go to New Member Training
IRBNet
IRBNet Training Energizer (PDF)
IRB Member eLearning Courses
- IRB Review Overview
- IRB Member’s Role
- Criteria for Approval
- Informed Consent Document Requirements
- Reviewing the Informed Consent Document
- IRB Actions
- Documenting the Review
- Researcher Outside Financial Interests in Research
- IRB Member Financial Information and Evaluations
Considerations for IRB Approval
Presenting Information for Effective Communication (Presented by Steven Woloshin, MD, MS and Lisa M. Schwartz, MD, MS) (Video, PDF)
Communicating Risks in the Consent Document (PDF)
Cognitively Impaired Adults in Research: Is greater than minimal risk acceptable? (PDF)
IRB Review of Medical Devices (PDF)
Choosing Determinations
- Module 1 – Criteria for Approval
- Module 2 – Vulnerable Populations
- Module 3 – Drugs and Devices
- Module 4 – Documentation
- Module 5 – Approval with Conditions
- Related Financial Interests and IRB Review
Institutional Review Board