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.

Presenters

Profile Picture for Dawn Corbett

Dawn Corbett

dcorbett@mail.nih.gov

NIH Inclusion Policy Officer
Office of Extramural Research (OER)
Office of the Director (OD)
NIH, HHS

Deysi Duque

deysi.duque@nih.gov

Human Subjects and Clinical Trials Specialist
Office of Extramural Research (OER)
Office of the Director (OD)
NIH, HHS

Rebecca Favor

rebecca.favor@nih.gov

Human Subjects and Inclusion Policy Specialist
Office of Extramural Research (OER)
Office of the Director (OD)
NIH, HHS

Profile Picture for Pamela Kearney

Pamela Kearney, M.D

pamela.kearney@nih.gov

Director
Division of Human Subjects Research (DHSR)
Office of the Director (OD)
NIH, HHS

Profile Picture for Lyndi Lahl

Lyndi Lahl

lyndi.lahl@nih.gov

Human Subjects Officer
Division of Human Subjects Research (DHSR)
Office of the Director (OD)
NIH, HHS

This page last updated on: October 12, 2024
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