IRB of Record. Informed consent must be obtained before the subject takes part in any aspect of the research study unless the IRB has approved a waiver of the requirement to obtain consent. ☐ Principal Investigator ☐ Qualified member(s) of the study team IMPORTANT: Consent should NOT be solicited immediately before beginning an elective procedure or scheduled therapy because the subject will not have time to consider whether to participate or not. When using DocuSign for electronic consent the subject must has access to their own computer, tablet, or smart phone. For security reasons, subjects should not use public or shared devices for signing e-informed consents. ►IF consent must be obtained the same day that study procedures commence, explain why the subject cannot be given more time to decide to consent and what will be done to ensure the potential subject has enough time to make an informed decision. ☐ N/A ☐ IN PERSON WRITTEN Informed Consent (on-site wet ink signature)
Appears in 2 contracts
Sources: Reliance Agreement, Reliance Agreement