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The IRB is offering this training session on choosing the right protocol template for your research project. This session targets study teams who plan to use the new Protocol Based Application for any of the following:
• Biomedical studies involving more than minimal risk OR multiple interventions
• Clinical trials
• Studies investigating drugs or devices
• Registry and Repository studies
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For registration questions, contact Emily Putman-Buehler (emily.putman@wisc.edu).
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IRBs staff
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Official Course Website
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No upcoming events.
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