Frequently Asked Questions

Q: What do I do to get started?
A: Go to our Getting Started page.

Q: I can't download the forms… what do I do now?
A: Contact the IRB Administrator, Laura Moll, and she will help you. You can send her Email at lmoll@clemson.edu or call her at 864-656-6460.

Q: I have some questions on the University's policies and regulations governing the use of human participants at Clemson University, who do I call?
A: You can contact the Office of Research Compliance at 864-656-6460.

Q: I am getting NIH funding. How do I sign up for the required training?
A: Please see our Online Training.

Q: My project has changed quite a bit. What do I do?
A: You will have to file an Amendment Request. That amendment will be reviewed by the IRB. The reviewers may then ask you to submit a new protocol depending upon how significant the changes actually are. Please remember that ALL changes should be reported to the IRB, no matter how insignificant you may think it is! This includes changes in study personnel, changes in expected participants, new advertising or promotions to recruit participants, changes to incentives offered, even the slightest change to the protocol, or even a one word change to the informed consent document. These must be reviewed and approved PRIOR to application or initiation.

Q: Can't I wait until the annual review?
A: No, as that would be out of compliance with Federal Regulations. Please contact the IRB Administrator for further assistance.

Q: My project is finished. Do I need to tell anyone?
A: Yes, please complete the Final Summary Report or contact the IRB Administrator as soon as possible.

Q: Do you still need help?
A: For additional questions, concerns, or suggestions, please contact our IRB Administrator at 864-656-6460.

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