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Big Data: Combining Registries and Legacy Clinical Trial Databases
Session Chair(s)
Michael J Pencina, PHD
Director of Biostatistics, Faculty Associate Director, Duke Clinical Research Institute, United States
This session will cover rare data, postmarketing, leveraging RWE, data sharing, open access, identifying cohorts for clinical trials, interoperability, differing standards, and submission considerations.
Learning Objective : Identify the potential of combining various types of studies and requirements to make it a success
Speaker(s)
Michael J Pencina, PHD
Director of Biostatistics, Faculty Associate Director, Duke Clinical Research Institute, United States
Supporting Open Access to Clinical Trials Data for Researchers: Challenges and Learnings
Michael Elashoff, PHD
CEO and Cofounder, Cornerstone AI , United States
Synthetic Control Arms: A Scientific Alternative to Historical Controls
Abel Kho
Director, Institute for Public Health and Medicine (IPHAM), Northwestern University, United States
Panelist
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