Videos
OHRP offers a collection of videos and webinars to help the research community better understand the HHS regulations for the protection of human subjects in research and their responsibilities for protecting human subjects. These materials are intended for public use and distribution, and we invite you to use and share them freely. We welcome you to link to our materials from your website.
Featured Videos
Simplifying Informed Consent (with OHRP)
November 10, 2020
Reporting to OHRP (1): Unanticipated Problems
November 10, 2020
OHRP Guidance on Response to COVID-19
April 28, 2020
When Does the Common Rule Apply? Review of the Basics Under the Revised Rule
June 22, 2018
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.
November 10, 2020
Reporting to OHRP (1): Unanticipated Problems
This video reviews the regulatory requirements for reporting unanticipated problems to OHRP, including how to determine when an unanticipated problem or adverse event must be reported.
April 28, 2020
The recorded videocast on OHRP’s COVID-19 Guidance
Short presentation by OHRP staff on WebEx platform, followed by moderated Q&A session.
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.
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. (November 10, 2020)
Content last reviewed on November 27, 2020
