University of Wisconsin–Madison
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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.

Instructor Info: 
Tracy Ohrt, Administrative Director, FDA Regulated Research Oversight Program, ICTR
Shari Zeldin, Clinical Research Compliance and IRB Officer, Department of Medicine

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

Register here

Details

Date:
November 13
Time:
12:00 pm - 1:00 pm
Event Categories:
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Venue

1345 Health Sciences Learning Center
750 Highland Avenue
Madison, WI 53705 United States
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