Frequently Asked Questions
The Frequently Asked Questions have been organized by topic.
- Whether IRB Approval is Needed
- IRB Review Types (how to select, differences)
- IRB Training
- Investigators (who can be PI, who to list)
- Guest Investigator Process
- Initial Application Process (forms, timing, notification)
- Supporting Documents (consent, instruments, formatting)
- Revisions (when, how)
- Renewal (when, how, how long does renewal last)
- Closure (when, how)
- Clinical Research Billing Compliance
- Unanticipated Problem Involving Risks to Subjects or Others
Many questions may also be answered by referring to the MSU HRPP Manual.
To submit a question, please email us at firstname.lastname@example.org.