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Research 6B – What Your Research Investigators and IRB May Not Know: Regulatory and Ethical Implications for Human Subjects Research

Level: Intermediate

Barbara Vimont, Director, Compliance and Privacy , Akron Children’s Hospital

Patricia Blount MD, MSL, CIP, CHRC, Managing Director, ProtocolsByDesign, LLC

  • Understand the fundamental difference between the practice of medicine and clinical research: The confusing roles of physician and clinical investigator
  • Understand the FDA regulatory landscape of sponsor-investigator INDs, nutraceuticals, and devices
  • Understand the fundamental difference between an interventional and observational study: Misperceptions concerning research interventions considered “standard of care” procedures

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9:00 am - 10:00 am


Jun 15 2021

Local Time

  • Timezone: America/New_York
  • Date: Jun 15 2021
  • Time: 10:00 am - 11:00 am