Review of QIU's Template Consent SOP
and How You Can Use It to Prevent Enrollment Deviations
![UCLA Research Administration Human Research Protection Program Logo](/sites/g/files/oketem271/files/styles/3_2_480x320/public/files/media/images/UCLA-Research-Administration-Human-Research-Protection-Program-Logo.jpg.webp?itok=HBcZKXqN)
Virtual
Hosted by: Clinical and Translational Science Institute (CTSI) and OHRPP
Presenter: Moore Rhys, OHRPP
To assist study teams with CAPAs for deviations relating to the consent process, OHRPP’s QIU has developed a template SOP that study teams can use to ensure a consistent process. This session will review the content of the template SOP (including why certain steps are included) and provide the template document for teams to use to prevent deviations.