DIA
Drug Information Association Logo
« Back to Listing

Patient Registries: Designing, Implementing, and Leveraging to Accelerate Clinical Trials

Track:
Clinical Operations

Day & Time:
June 17, 3:30PM - 5:00PM (Pacific Standard Time)

Session Number:
282

Room Number:
3

Level:
Intermediate

Type:
Session

Title:
Patient Registries: Designing, Implementing, and Leveraging to Accelerate Clinical Trials

Chair(s):
Lisa Palladino Kim, MS
Global Trial Optimization Specialist
inVentiv Health Clinical, United States

Description:
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(s):
Identify the methodology used to design and implement a patient registry; Illustrate how registries accelerate clinical trials and incorporate the patient voice into research.

Presentation(s) & Speaker(s):
Beyond the RFP: Driving Value Through Effective Registry Strategy, Design, and Operations
Leanne Larson
Vice President and Global Head, Observational Research
PAREXEL International, United States

Incorporating Patient Voice to Speed Development Using Rare Disease Registries
MJ Schmidt
Vice President, Business Development
Engage Health, Inc., United States

Bridging Patient Registries to Clinical Research: A Win-Win Opportunity
Thomas A. Krohn
Advisor, Clinical Open Innovation
Eli Lilly and Company, United States