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Session 8: Real-World Data in the Real World: How to Operationalize the Data Journey
Session Chair(s)
Jaclyn Bosco, PhD, MPH, FISPE
Vice President, Global Head of Epidemiology & Database Studies
IQVIA, United States
The expectations from regulators and other decision-making stakeholders are increasing for the use of real-world data to generate valid and robust evidence. Putting theory into practice has evolved using new technology and methods to improve our operational execution of real-world study protocols. This session will provide practical applications for the data journey from abstraction, linkage, programming and reporting to increase the quality of real- world evidence generation.
Learning Objective : - Understand the benefits and risks of human-only, AI-only, and human-in-the-loop AI-enabled data abstraction
- Apply concepts from software engineering to avoid errors throughout the lifecycle of a study and ensure reproducibility
- Describe considerations and demonstrate data management steps for linking administrative claims data with clinical trial data using tokenization
Speaker(s)
AI-Enabled Data Abstraction: Benefits and Risks for Data Curation
Troy Astorino
PicnicHealth, United States
CTO
Seeing Eye to Eye: Enhancing Inter-Team Communication for Reproducible Real World Evidence
Nuvan Rathnayaka
Target RWE, United States
Manager of Biostatistics
Supplementing the Identification of Clinical Endpoints through Tokenization of Clinical Trial Participants
Claudia Salinas, PhD
Eli Lilly and Company, United States
Senior Director, GPS Pharmacoepidemiology
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