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Implementation of eConsent and Other Digital Clinical Trial Innovations
Session Chair(s)
Cassandra Smith, MBA
Director, Diversity, Equity, and Inclusion in Clinical Trials
Janssen Research & Development, United States
Learn about using eConsent in the informed consent process. Insight will be shared into understanding how eConsent may be used to improve the consent process; how this may impact sites, IRBs, and sponsors; and how the use of eConsent may impact the patient experience. Finally, attendees will learn how to use other digital tech innovations to advance patient centricities.
Learning Objective : Describe how eConsent may be used to improve the entire consent process including the improving the patient experience in clinical trials; Discuss available resources to support implementation of eConsent for sites, IRBs, and sponsors; Analyze findings from surveys and pilots to understand eConsent experience; Explain how data platforms are supporting stakeholders flexibility to advance patient centricity powered digital tech innovations, accelerate study design, and improve data quality.
Speaker(s)
Transforming Informed Consent: Current Landscape and Tools to Enable the Future of eConsent
Cassandra Smith, MBA
Janssen Research & Development, United States
Director, Diversity, Equity, and Inclusion in Clinical Trials
Driving Clinical Outsourcing Innovation Forward with Machine Learning: Self-Driving Systems to Automate and Accelerate
MaryAnne Rizk, PhD
Rizk Management Advisors, United States
Chief Executive Officer
eConsent: A Patient-Centric Program to Improve Enrollment, Recruitment, and Retention
Eric Delente, MA
Self-employed, United States
Consultant
Are Your Sites Prepared for eConsent?
Cami Gearhart, JD
Quorum Review IRB, United States
CEO
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