{"templateJson":{"children":[{"dataId":1801362,"name":"Section3","text":"Identify type of Review","label":"","type":"question","children":[{"dataId":1801363,"name":"Group3","text":"","description":"After checking appropriate option, navigate to the next page to begin. Complete all applicable questions. Incomplete submissions will be returned. Refer to help text throughout the submission for additional information and guidance. When complete, click submit, and then click Certify. (when there is a Faculty Sponsor, the Faculty Sponsor will also need to certify)","required":false,"helpText":"If you are planning to conduct research with human subjects, complete the Initial IRB Review Request Form to request IRB review.
If you are unsure whether your project requires IRB review, submit a Not Human Subjects Research determination request.
If you are collaborating with researchers at another institution whose IRB has reviewed the project and will act as the IRB of record, submit a Request to Rely on External IRB.
","compoundType":"checkbox","label":"","type":"question","children":[{"dataId":1801364,"name":"CheckBox3","text":"Initial IRB Review Request Form","required":false,"helpText":"","label":"","type":"checkbox"},{"dataId":1801365,"name":"CheckBox4","text":"Request for Determination of Human Subjects Research
(if you are unsure if your project requires IRB review)","required":false,"helpText":"","label":"","type":"checkbox"},{"dataId":1801366,"name":"CheckBox5","text":"Request to Rely on External IRB
","required":false,"helpText":"","label":"","type":"checkbox"}]}]},{"dataId":1801367,"name":"Section11","text":"PI Assurance","label":"1.1","type":"question","dependencies":[{"targetId":1801365,"type":"displayed"},{"targetId":1801364,"type":"displayed"},{"targetId":1801366,"type":"displayed"}],"children":[{"dataId":1801368,"name":"Group18","text":"All projects that meet the definition of research with human subjects (45 CFR 46.102) must be reviewed and approved by the IRB, or receive an exempt determination, prior to beginning the research. Submissions are initially screened by IRB staff to determine completeness and appropriate type of review. Submissions may be returned to the study team for changes before the review type is assigned. The review type may be reassessed at any time during the review process.","description":"*Submissions requiring full committee review must be received at least 30 days prior to the scheduled committee meeting to allow time for pre-review. The IRB meets as needed during the regular academic year. IRB meeting schedule is posted here.
*Submissions requiring Exempt or Expedited review will be reviewed in the order received.
For more information about the IRB submission Process, IRB Tracking, and Kennesaw IRB Tasks, please refer to the Kennesaw IRB Website.","required":false,"helpText":"","label":"","type":"question"},{"dataId":1801369,"name":"Label6","text":"Principal Investigator's Assurance Statement
I certify that the information provided in this application is complete and accurate.
I understand that as principal investigator, I have ultimate responsibility for the conduct of the study, the ethical performance of the project, the protection of the rights, safety and welfare of the human subjects, and strict adherence to the study protocol and any conditions or modifications stipulated by the KSU IRB.
I will submit modifications of the protocol and/or the informed consent form and/or any other documents to the IRB for approval prior to applying those changes in the study as required.
I agree to abide by the policies and procedures of the KSU IRB regarding the protection of human subjects including, but not limited to: