UCLA Research Administration Human Research Protection Program Logo
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.