Mailed consent materials may be returned incomplete or incorrectly completed. If documents will be returned to the subject for corrections,the research team must describe how this will occur in Sections VII.D.29 (for adults) and/or VII.D.30 (for parents/guardians of minors) in HawkIRB. Researchers can generate the template, edit and attach the letterin the miscellaneous category on the Attachments page of HawkIRB. Investigators utilizing a mailed consent process may also tailor the signature block of ICD so the research team can indicate whether consent was obtained in person, over the phone, or if no conversation took place between a member of the research team and the subject.
Please be sure to generate your template in HawkIRB, not from this web example.