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Human Subjects Research: Policies, Clinical Trials, & Inclusion - Day 1 - Video
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- What are the basic HHS regulations and NIH policies that apply to research involving human subjects, including clinical trials?
- How do you prepare a research proposal for review that addresses the regulatory requirements?
- What are some strategies for developing realistic and scientifically acceptable inclusion plans?
Join experts from the NIH Division of Human Subjects Research and HHS Office of Human Research Protections (OHRP) for answers to these questions and additional valuable information and resources. During this 2-day event, these NIH and HHS experts will share policies, resources, guidance, and case studies in this informative and engaging, live event.
Full transcript (DOCX, 136.22 KB)
How Do I Know if a Research Study is Human Subjects Research (PPTX, 1.94 MB)
What You Need to Know About FWAs and IRBs (PPTX, 6.22 MB)
An Overview of NIH Policies on Human Subjects Research (PPTX, 3.57 MB)
Essentials of sIRB Requirements (PPTX, 3 MB)
Presenter(s)
Marianna Azar
Public Health Program Specialist
Office for Human Research Protections (OHRP)
Division of Education and Development
HHS
Dawn Corbett
NIH Inclusion Policy Officer
Office of Extramural Research (OER)
Office of the Director (OD)
NIH, HHS
Deysi Duque
Human Subjects and Clinical Trials Specialist
Office of Extramural Research (OER)
Office of the Director (OD)
NIH, HHS
Rebecca Favor
Human Subjects and Inclusion Policy Specialist
Office of Extramural Research (OER)
Office of the Director (OD)
NIH, HHS
Pamela Kearney, M.D
Director
Division of Human Subjects Research (DHSR)
Office of the Director (OD)
NIH, HHS
Lyndi Lahl
Human Subjects Officer
Division of Human Subjects Research (DHSR)
Office of the Director (OD)
NIH, HHS