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Patient Registries: Designing, Implementing, and Leveraging to Accelerate Clinical Trials
Session Chair(s)
Lisa Palladino-Kim, MS
Program Director / Lecturer
Rutgers School of Health Professions Clin Research Mgmt, United States
This session will examine how the biopharmaceutical industry, academic organizations, and patient advocacy groups value and utilize patient registries in clinical trials. We will discuss areas of controversy and best practices.
Learning Objective : Identify the methodology used to design and implement a patient registry; Illustrate how registries accelerate clinical trials and incorporate the patient voice into research.
Speaker(s)
Beyond the RFP: Driving Value Through Effective Registry Strategy, Design, and Operations
Leanne Larson
Parexel International, United States
Senior Vice President, WW Head Real-World Evidence and Access
Incorporating Patient Voice to Speed Development Using Rare Disease Registries
MJ Schmidt
Engage Health, Inc., United States
Vice President, Business Development
Bridging Patient Registries to Clinical Research: A Win-Win Opportunity
Thomas A. Krohn, RPh
Antidote, United States
Chief Development Officer
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