All new IRB submissions must be entered using the new system.
- Access eRIA-IRB
eRIA-IRB upgrade is now available for use.
If you have any questions or need assistance, please feel free to reach out to our eRIA IRB team. Our goal is to help make the transition to a more efficient online system a smooth one!
Use this template to develop Informed Consent Forms and note that an informed consent is required for most prospective research with human subjects.
- Standard Adult Consent (.pdf)
- Standard Adult Consent (.doc)