IRB Forms
| Amendment Form | Used to apply for approval to change or add to your project in any way. For example: Protocol changes, personnel changes, advertisements, enrollment numbers, etc. |
| Continuation Form | Your approval period is listed on your IRB approval letter. If your research takes longer than your approval period, please use this application to continue approval for your project. |
| Closure Form | Use this form to close your research study with the IRB when you are finished. |
| Cognitively Impaired or Persons Unable to Consent Form |
Used to justify involving this protected group of subjects
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| Tracking Log for Nonreportable Events | Used to report events other than Unanticipated problems |
| Unanticipated Problems Form | For reportable problems that are unanticipated, related, and serious |
| Financial Disclosure Form B | Used to disclose a financial interest in the research or sponsor. |
| Location Site Form | Used for medical studies only, to verify site participation. |
| Specimen Collection Checklist | Attach to application when banking specimens for future use. |
| Emergency Use of a Test Article | Used to evaluate if emergency use of a test article is appropriate. |
| Call office for details. 605-677-6067 | |
| HIPAA Authorization | Addendum to Informed Consent |
| HIPAA Partial Waiver of Authorization Form | Use for recruitment purposes |
| HIPAA Full Waiver of Authorization Form | Use for chart review projects |
| HIPAA PHI of Decedents Form | Use to apply for use of decedent PHI |