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What Your Research Investigators and IRB May Not Know: Regulatory and Ethical Implications for Human Subjects Research
Barbara Vimont, Director, Compliance and Privacy, Akron Children's Hospital. Patricia Blount MD, MSL, CIP, CHRC, Managing Director, ProtocolsByDesign, LLC.
June 15, 2021
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Understand the fundamental difference between the practice of medicine and clinical research: The confusing roles of physician and clinical investigator
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Understand the FDA regulatory landscape of sponsor-investigator INDs, nutraceuticals, and devices
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Understand the fundamental difference between an interventional and observational study: Misperceptions concerning research interventions considered "standard of care" procedures
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