Consent Forms. Provide the Reviewing IRB with the site-specific information requested/identified in the customizable sections of the Reviewing IRB’s consent form, for review and approval by the Reviewing IRB, when written informed consent is required. Once the consent form is approved for use by the Relying Institution/Site Investigator(s), the Relying Institution will not, and will require that its Site Investigator(s) not, make any change to the form without obtaining prior approval of that change from the Reviewing IRB.
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Samples: Smart Irb Joinder Agreement, hso.research.uiowa.edu, smartirb.org