Uploaded November 2020 | Updated September 2026, 1 week ago
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.
Recorded on October 30, 2020 during session at 2020 NIH Virtual Seminar on Program Funding and Grants Administration.
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.
Recorded on October 30, 2020 during session at 2020 NIH Virtual Seminar on Program Funding and Grants Administration.
