Printer-friendly version
When a template consent document is available from the study sponsor, the investigator should attach it in the Miscellaneous attachments category of the HawkIRB application. The template should be attached even if the investigator is not proposing to use the template consent to enroll subjects.
A complete submission for IRB review includes sample Informed Consent Document(s). When federally funded and available from the industry or federal (DHHS, NIH, FDA, etc.) sponsor, the IRB must be provided with the template consent document to review any deviations.