RETHINK CLINICAL TRIALS
Increase the success of your clinical program by connecting study data with real-world data at the patient level
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LEARN MORE FROM TRIALS
Better understand outliers and follow outcomes even after a study is complete
GAIN FLEXIBILITY
Answer the questions you didn’t think to ask when the trial was designed
CUT YOUR COSTS
Reduce the need for site visits and lose fewer patients to follow-up
Connect to the nation's largest ecosystem of real-world data to support:

RETROSPECTIVE COHORT ANALYSIS
Understand study outliers and the outcomes of patients lost to follow-up
POST-MARKETING STUDIES
Lower the costs of monitoring for long-term safety and efficacy
HYBRID STUDIES
Join data collected through trials and RWD sources for a more holistic view of the patient
SYNTHETIC CONTROLS
Reduce time and costs by incorporating RWD sources and pragmatic design
How it Works
Datavant Patient Keys act as a unique, consistent ID that can be used to match a consenting patient’s study data to their data in the real world, without unblinding the study

Datavant provides us with a broad array of built-in connections to real-world data sources, which can now be combined to yield a more holistic view of patient health than clinical trial data alone.
Dr. Michelle Longmire
Resources
White Paper
Trial Tokenization

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Webinar
Using RWD in Clinical Development

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White Paper
Datavant & Parexel Use RWD for Clinical Research

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Case Study
External Control Arms
