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Human Subjects Research: Policies, Clinical Trials, & Inclusion - Day 2 - 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 the HHS Office of Human Research Protections (OHRP) for answers to these questions and additional valuable information and resources. During this 2-day virtual event, NIH and HHS experts will share policies, resources, guidance, and case studies.
Full transcript (DOCX, 157.23 KB)
An Overview of NIH Policies on Clinical Trials (PPTX, 3.54 MB)
Including Diverse Populations in NIH Research (PPTX, 2.6 MB)
Using the Human Subjects System (HSS) (PPTX, 4.54 MB)
Presenter(s)
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