How to Write an Informed Consent Form
October 30 @ 1:00 pm - 2:00 pm
This presentation will review the new Informed Consent Form templates developed by the Health Sciences IRB Office, as well as common errors that can be prevented when writing an informed consent document.
Tina Graber, Regulatory Specialist, Office of Clinical Trials
Jennifer Fenne, Senior IRB Analyst, HS IRB
Emily Putman-Buehler, email@example.com