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Frequently Asked Questions

Please see the topics below for frequently asked questions about conducting a human participant research study.

Do I Need to Submit?
Frequently asked questions about when a submission to the Institutional Review Board (IRB) is required
Before/During the Review Process
Frequently asked questions about the Institutional Review Board (IRB) review process
After Submitting the Proposal and Approval is Granted
Frequently asked questions about ongoing actions post Institutional Review Board (IRB) approval
Informed Consent
Frequently asked questions about informed consent
Continuing Reviews
Frequently asked questions about Institutional Review Board (IRB) continuing reviews
Contact us

Staff Directory and About Us...
814-865-1775
The Human Research Protection Program in the Office for Research Protections ensures compliance with Federal, state, and local regulations as well as institutional policies and procedures regarding the use of humans as participants in research.