New Course – OHRP: Participant-Centered Informed Consent Training

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Description

This training will help the research community create, design, and review consent forms or templates for research participation in a way that helps participants understand the content and anticipate their needs. This participant-centered approach helps people understand the research and how the decision to participate or not might impact them personally.

This course is meant to supplement basic human subjects research training covered in CITI Program’s Human Subjects Research (HSR) series.

Note: This course is only available for subscribing organizations who utilize the HSR series. The course is available at no additional charge.

 


Audience

IRB Administrators and Staff, IRB Chairs, IRB Directors, IRB Members, Legal/Compliance Staff

 


Disclaimer

The material is a faithful, unchanged (other than reformatting to fit the CITI Program platform) duplication of the Department of Health and Human Services (HHS) Office for Human Research Protections’ (OHRP’s) INTERACTIVE PARTICIPANT-CENTERED INFORMED CONSENT TRAINING program, released on February 7, 2024. It is available here at no additional charge. While the CITI Program and the OHRP Trainings are identical in substantive content, OHRP is not responsible for the accuracy of the content reproduction, operation, or record keeping related to the INTERACTIVE PARTICIPANT-CENTERED INFORMED CONSENT TRAINING program on the CITI Program website and does not endorse CITI Program or any of its products or services.