IRB Application for Human Participant Research听
- Use this form to submit a new human subject research protocol to the IRB.
- This is a Microsoft Word form with fillable fields.
- DO NOT use it as a Google Doc or in a Google Drive
Download Here:听IRB Application Form 7.1
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IRB Revision Request Form
- Used to request a change to a previously approved or exempted IRB protocol.
- This is a Microsoft Word form with fillable fields.
- DO NOT use it as a Google Doc or in a Google Drive
Download Here: IRB Revision Request Form 4.0
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IRB Continuation Request听Form
- Used to extend the approval period for an IRB protocol
- Continuing Review is not always required for minimal-risk IRB protocols. Refer to the Notice of Approval document for the approval expiration date of your protocol.
- Must be submitted 4-5 weeks BEFORE the approval expiration date
- If an approved protocol expires, research must CEASE IMMEDIATELY
Download Here: IRB Continuation Request Form 6.0
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Individual Investigator Agreement (IIA)
- Researchers who are external to 糖心logo在线入口 must submit this form with their completed IRB Application for Human Subject Research.
- Please see the IRB Administrator for specific instructions.
Download Here: 糖心logo在线入口 Individual Investigator Agreement
糖心logo在线入口 Informed Consent/Assent Documents
First: Review
- Adult Informed Consent Template听(non-exempt studies, a signature is required)
- Minimal Risk Study Information Page听Template听 (Perfect for PS301/401 students.)
- Online Survey Consent Template听 (Excellent for use in Qualtrics surveys!)