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![OHRP: What is Human Subjects Research? Part 1: A Review of the Common Rule and Its Application](https://public3.pagefreezer.com:443/content/HHS.gov/08-12-2021T10:43/https://www.hhs.gov/ohrp/sites/default/files/video-thumb.png)
OHRP: What is Human Subjects Research? Part 1: A Review of the Common Rule and Its Application
November 17, 2021
![OHRP: What is Human Subjects Research? Part 2: What Investigators Should Know About IRB Review](https://public3.pagefreezer.com:443/content/HHS.gov/08-12-2021T10:43/https://www.hhs.gov/ohrp/sites/default/files/video-thumb.png)
OHRP: What is Human Subjects Research? Part 2: What Investigators Should Know About IRB Review
November 17, 2021
![Use of eConsent in Human Subjects Research](https://public3.pagefreezer.com:443/content/HHS.gov/08-12-2021T10:43/https://www.hhs.gov/ohrp/sites/default/files/video-thumb.png)
Simplifying Informed Consent (with OHRP)
November 10, 2020
![Making Mobile Clinical Trials a Reality](https://public3.pagefreezer.com:443/content/HHS.gov/08-12-2021T10:43/https://www.hhs.gov/ohrp/sites/default/files/video-thumb.png)
When Does the Common Rule Apply? Review of the Basics Under the Revised Rule
June 22, 2018
November 17, 2021
OHRP: What is Human Subjects Research? Part 1: A Review of the Common Rule and Its Application
This two-part session explains how to prepare a research proposal that addresses the regulatory requirements for review including the requirements for informed consent and helps investigators understand their responsibilities with respect to IRB review and protections of human research participants.
November 17, 2021
OHRP: What is Human Subjects Research? Part 2: What Investigators Should Know About IRB Review
This two-part session explains how to prepare a research proposal that addresses the regulatory requirements for review including the requirements for informed consent and helps investigators understand their responsibilities with respect to IRB review and protections of human research participants.
November 10, 2020
Simplifying Informed Consent (with OHRP)
In this session, representatives from the Office for Human Research Protections (OHRP) will discuss what goes into a meaningful informed consent. Practical examples will be used to illustrate how to discern meaningful information for potential participants, and how to present information simply in consent documents and materials to ensure consent processes fulfill their goal of enabling potential participants to make informed decisions about whether to participate in the research.
June 22, 2018
When Does the Common Rule Apply? Review of the Basics Under the Revised Rule
This video reviews the revised Common Rule and how to determine when a research study is considered nonexempt human subjects research under the revised Rule. The presentation also includes a brief introduction of the exemptions.