- IRB Determination Form - This form should be completed and submitted if you are unsure if your project requires IRB approval.
- Amendments or Changes to Study Procedures Form - All amendments and changes must be reviewed and approved by the IRB before they are implemented.
- Institution Authorization Agreement Request Form - use this form if you are requesting that the KSU IRB serve as the IRB of record for a multi-institution project, or if you are requesting that another Institution's IRB serve as the IRB of record for your project.
- Annual Review Form
- Closeout Form
- Event Form - Use this form if you are reporting an adverse events, complaints from participants, etc. to the IRB.
Information about HIPAA
- HIPAA Authorization Template
- Requirements for an Authorization Form for HIPAA Compliance
- Class Project Parameters and Forms
- Action Research Parameters and Forms
- Web-based study information
- Procedures for Compensating Research Participants
International Human Research Protections
- International compilation of Human Research Protections - a listing of over 1,000 laws, regulations, and guidelines on human subjects protections in over 100 countries and from several international organizations.
List of Additional Application Materials:
||Addition of Co-PI or Key Personnel|
||Addition of External Co-PI or Key Personnel|
||Drugs and Biologics|
||Biological Specimens Repository|
||Non-English Speaking Participants|
||Waiver of Alteration of Consent Process|
||Waiver of Consent Documentation|
||Collection of Family History Data|
||Blood, Injections, or Surgical Procedure|
||Adverse Event Involving Risks to Subjects or Others|
||Change in Principle Investigator
||Adults with Decisional Impairment|
|Appendix Y||Student Recruitment Online Pools|
||Conflict of Interest for Human Subjects Research|