- Exempt Study Informed Consent Template
Exempt studies Informed Consent Template
This template is to be used for exempt studies only, as defined here and in the Core Info Section of the Cayuse Protocol. Use of this form for an expedited or full board category study will result in the study being returned and a new informed consent document will be required. Please click here for more details on review categories
- Expedited/Full board Consent Templates
Please click here for more details on review categories
Informed Consent Form - Adults - The consent form used for most studies that require a signature.
Informed Consent and Assent Forms - Parents and Minors - Parental consent/permission and child assent forms that are used for studies enrolling minors.
Informed Consent Form- With HIPAA Authorization - A consent form used when medical information (HIPAA) will be collected.
Informed Consent Notice - Electronic Consent - Consent form used for electronic surveys.
- Recruitment Templates
Recruitment Message - An example of an email used to recruit participants for a human subjects research study. All elements of the template must be included but you may format the email as you wish.
Recruitment Flyer - A recruitment flyer seeking participation in a human subjects study. All elements of the template must be included but you may format the flyer as you wish.
- Request for Consent Alteration/Consent Waiver
Request for Consent Alteration/Consent Waiver - Required form if you are using the Informed Consent Notice- Electronic Consent form
- Final Report
IRB Final Report - Request to terminate an active study. This form should be attached to a Cayuse "Closure" request.
- Cayuse submission help document
Cayuse submission help - Cayuse IRB Initial Submission Guide
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