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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.
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Emily Putman-Buehler (emily.putman@wisc.edu)
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Tracy Ohrt, Administrative Director, FDA Regulated Research Oversight Program, ICTR
Shari Zeldin, Clinical Research Compliance and IRB Officer, Department of Medicine
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Official Course Website
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No upcoming events.
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