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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)
Supporting Open Access to Clinical Trials Data for Researchers: Challenges and Learnings
Michael J Pencina, PhD
Duke Clinical Research Institute, United States
Director of Biostatistics, Faculty Associate Director
Synthetic Control Arms: A Scientific Alternative to Historical Controls
Michael Elashoff, PhD
Cornerstone AI , United States
CEO and Cofounder
Panelist
Abel Kho
Northwestern University, United States
Director, Institute for Public Health and Medicine (IPHAM)
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