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How to Obtain Informed Consent (the process)  (back)
 
Description:
This presentation will review the important, basic concept of the informed consent process. This training is geared towards the newer members of the study team or those that are looking for a refresher.
Contact Info:
Emily Putman-Buehler (emily.putman@wisc.edu)
Instructor Info:
Tracy Ohrt, Administrative Director, FDA Regulated Research Oversight Program, ICTR
Shari Zeldin, Clinical Research Compliance and IRB Officer, Department of Medicine
 
Official Course Website
 
No upcoming events.

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