Forms related to the IRB process. All forms are available in MS Word format. If you do not have Microsoft Word on your computer, you can download the Word Viewer.
- Adverse Incident Reporting Form
Must be completed any time a research subject experiences an adverse reaction to or unexpected event following an intervention by a research as part of an IRB protocol.
- Annual Review Form Human Subjects Research Projects
- Research Project IRB Application Form
- HIPAA Authorization Form and Appendix A
Form and guidelines for compliance to the Health Insurance Portability and Accountability Act as it relates to the protection of health information.
- Research Closure Form
Form to inform IRB board of the completion of previously approved research.
- Research Modification Form
Form to request changes of substantive details to a previously approved research.
- Research Study Assent Form Under 18 Years of Age
Form to provide information and acquire consent from research participants under 18. This form is to be used with the Research Student Parent Permission form.
- Research Study Consent Form
Form to provide information and acquire consent from research participants.
- Research Student Parent Permission Form
Form to provide information and acquire consent from research participants under age 18 through their parents or guardians. This form is to be used with the Research Study Assent form under 18 years of age.
- Elements of Informed Consent
Informed consent form must include these elements in sequential order and in language which the participants can understand.