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How to Obtain Informed Consent (the process)
November 13 @ 12:00 pm - 1:00 pm
This presentation will review the important elements of the informed consent process.
Tracy Ohrt, Administrative Director, FDA Regulated Research Oversight Program, ICTR
Shari Zeldin, Clinical Research Compliance and IRB Officer, Department of Medicine
Emily Putman-Buehler, firstname.lastname@example.org