We designed and evaluated an integrated process for gaining broad consent for research using only clinic staff. By using standard patient registration workflow as a template, we established the Biospecimen Use for Research Related Investigations and Translational Objectives (BURRITO) framework which can be adapted to a broad range of existing out-patient clinical environments seeking to standardized research consent into the Electronic Medical Record.
Learning Objective 1: Evalute a process of obtaining broad consent for clinical remnant samples that is integrated into standard clinical registration workflows in an out-patient healthcare environment
Stephanie Soares (Presenter)
University of California, Davis
Nick Anderson, University of California, Davis
Leslie Solis, University of California, Davis
Javier Lopez, University of California, Davis