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.
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.
Investigator Agreement

Investigator Agreement-No FWA
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.