Human Subjects Research: Policies, Clinical Trials, & Inclusion - Day 2
Event Overview:
Description:
- 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.
Objective:
- Gain a better understanding of HHS regulations and NIH policies that apply to research involving human subjects and clinical trials
- Obtain guidance on how to prepare a research proposal for review addressing regulatory requirements
- Learn strategies for developing realistic and scientifically acceptable inclusion plans
Event Resources
- 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)
See Also
On-Demand Videos:
Podcasts:
- All About Grants Podcasts (Link pre-filtered for Clinical Trials, Human Subjects, and Inclusion topics)
Documents:
- Resources: Human Subjects Protections, Inclusion, and Clinical Trials (Includes links to Policies, Notices, Tools, Resources, & Training on the following: Human Subjects Protections, Clinical Trials, Inclusion, General Information)
Website Links:
- NIH Human Subjects Research Home Page
- NIH Inclusion Policies Home Page
- NIH Single IRB for Multi-Site or Cooperative Research Page
- NIH Certificates of Confidentiality (CoC) Page
- NIH Clinical Trial Policies Home Page
- Basic Experimental Studies Involving Humans (BESH) Page
- HHS Office for Human Research Protections (OHRP) Page
- eRA Human Subjects System (HSS) Resource Page
Agenda
Welcome & Overview | |
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12:00 pm ET Moderator: Lyndi Lahl, R.N., M.S., NIH Human Subjects Officer, Office of Extramural Research (OER), NIH |
An Overview of NIH Policies on Clinical Trials | |
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12:10 pm ET Moderator: Lyndi Lahl, R.N., M.S., NIH Human Subjects Officer, Office of Extramural Research (OER), NIH Presenter: Pamela Kearney, M.D., Director, Division of Human Subjects Research, Office of Extramural Research (OER), NIH |
Including Diverse Populations in NIH Clinical Research | |
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01:30 pm ET Moderator: Rebecca Favor, DrPH, C.P.H., NIH Human Subjects and Inclusion Policy Analyst, Office of Extramural Research (OER), NIH Presenter: Dawn Corbett, M.P.H., NIH Inclusion Policy Officer, Office of Extramural Research (OER), NIH |
Using the eRA Human Subjects System (HSS) | |
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02:30 pm ET Moderator: Dawn Corbett, M.P.H., NIH Inclusion Policy Officer, Office of Extramural Research (OER), NIH Presenter: Rebecca Favor, DrPH, C.P.H., NIH Human Subjects and Inclusion Policy Analyst, Office of Extramural Research (OER), NIH |
Continuing the Conversation with NIH & HHS Human Subjects Experts | |
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03:15 pm ET *Includes all NIH & HHS presenters from Day 1 and Day 2 Moderator: Deysi Duque, M.S, PMP., NIH Human Subjects and Clinical Trials Specialist, Office of Extramural Research (OER), NIH |
Presenter(s):
Contact:
FAQs
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Accessibility
The NIH Office of Extramural Research strives to host inclusive, accessible events that enable all individuals to engage and participate fully.
All live, virtual events include closed captions. Reasonable accommodation requests should be submitted in advance at least 5 days prior to an event to [email protected].
Respect
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