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Presenters will go over key considerations for documenting informed consent: what “counts” as documentation, which regulatory determinations are required and how to request them, remote consent processes, exemption requirements, and what to consider if assent, HIPAA, or FDA regulations apply. There will also be time for Q&A.
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prep@research.wisc.edu
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Jackie Lee, MRR IRB; Jennifer Fenne, HS IRB; Jake Rome, FDA Regulated Research Oversight Program
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Official Course Website
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No upcoming events.
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