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This course will describe various options for obtaining remote consent, including how to set up and use DocuSign. Attendees will hear a study coordinator's perspective on obtaining remote consent and learn more about regulatory considerations for remote consent.
A WebEx link will be sent to attendees the day before the course.
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Emily Putman-Buehler (emily.putman@wisc.edu)
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Tina Graber, Office of Clinical Trials
Meg Hackbarth, Office of Clinical Trials
Anna Martin, Health Sciences IRBs
Danae Wolff, UW Carbone Cancer Center
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Official Course Website
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No upcoming events.
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