University of Wisconsin–Madison
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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.

Instructor Info: 
Tina Graber, Regulatory Specialist, Office of Clinical Trials
Jennifer Fenne, Senior IRB Analyst, HS IRB

Contact Info: 
Emily Putman-Buehler, emily.putman@wisc.edu

Register here

 

Details

Date:
October 30
Time:
1:00 pm - 2:00 pm
Event Categories:
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Venue

1335 Health Sciences Learning Center
750 Highland Avenue
Madison, WI 53705 United States
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