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ON DEMAND - Templates That Do More: How We Are Accelerating Drug Development via Structured Content Reuse
Session Chair(s)
Mitzi Allred, PHD
Director, Clinical Operations
Merck & Co., Inc, United States
This session explores the emerging digitization of medical regulatory documents templates. With these templates structure dictates for improved quality, comprehension, reuse, and enabling technology for speed and quality.
Learning Objective : Discuss the benefits of smart templates and how they enable content for multiple uses; Describe the impact on speed when intelligence and digitation are applied to the templates; Compare and contrast traditional narrative driven templates vs. the need for speed and digitization.
Speaker(s)
Templates That Do More: A Story Told With the NIH eProtocol Tool
Alyssa Tonsing-Carter, PHD
National Institutes of Health (NIH), United States
Health Science Policy Analyst, Office of the Director, Office of Science Policy
Accelerating Drug Development via Structured Content Reuse: Introducing eTemplates
Vivian Combs, MS
Eli Lilly and Company, United States
Executive Director, Clinical Trial Foundations
Templates That Do More: Why Structured Documents Matter! A Story Told With eTemplates
Mitzi Allred, PHD
Merck & Co., Inc, United States
Director, Clinical Operations
Industry Update
TK Booker Porter, PHD
Greenwich BioSciences, United States
Senior Director, Global Medical Writing and Regulatory Operations