The Michigan Institute for Clinical & Translational Research (MICHR) provides supplemental training on the basics of electronic informed consent. This self-guided course is about the process of using electronic consent (eConsent) for clinical and translational research and was designed to outline basic concepts study team members should consider before using eConsent processes. Participants will learn what eConsent is and how it can be operationalized by study team members.
This training is designed to supplement synchronous workshops on the basics of informed consent provided by the Michigan Institute for Clinical and Health Research. No prior research experience or technical background is necessary to take this course, but further training on informed consent is recommended for all participants.