Description
The eIC platform was developed to augment educational alternatives for research participants, reduce administrative time/effort associated with paper-based consenting, improve the IC audit trail, and streamline consent document authoring for clinical research studies. The platform provides an innovative operational model for electronic consenting in the academic medical setting, enhances the engagement and education of study participants, and improves quality and compliance in the consent process.
Learning Objective: Understand the current issues in the electronic consenting landscape in the academic medical setting.
Learn the challenges and advantages of having electronic consents being sent directly to the electronic health record system; from an auditing, compliance, regulatory, and workflow streamlining perspective.
Understand the quality of the electronic informed consent process from participant feedback.
Formulate an approach for adoption of electronic informed consenting at an academic medical site.
Authors:
Michael Buckley (Presenter)
Memorial Sloan Kettering Cancer Center
Joseph Lengfellner, Memorial Sloan Kettering Cancer Center
Matthew Koch, Memorial Sloan Kettering Cancer Center
Hector Pacheco, Memorial Sloan Kettering Cancer Center
Carol Hoidra, Memorial Sloan Kettering Cancer Center
Dorothy Damron, Memorial Sloan Kettering Cancer Center
Collette Houston, Memorial Sloan Kettering Cancer Center
Roy Cambria, Memorial Sloan Kettering Cancer Center
Ann Rodavitch, Memorial Sloan Kettering Cancer Center
Paul Sabbatini, Memorial Sloan Kettering Cancer Center
Presentation Materials: