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Life Sciences

Real-World Evidence
at the Scale You Need

One of the nation's largest real-world clinical datasets: 300M+ patient records, 40B+ data points, from 6,000+ practices across the country.

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Core Capabilities

From hypothesis to
evidence — faster

Accelerate drug development, post-market surveillance, and clinical trial recruitment with clinical data that's already structured, coded, and ready.

300M+ Patient Records
Longitudinal patient data from ambulatory practices nationwide — including diagnoses, medications, procedures, labs, and vitals — going back 20+ years.
EHR-Linked Practice Network
Data sourced directly from EHR systems at 6,000+ practices, with high data fidelity because it was captured at the point of care — not from claims.
ePRO & Clinical Trials
Recruit qualified patients from our network for decentralized and hybrid clinical trials. ePRO tools capture patient-reported outcomes efficiently.
Longitudinal Patient Tracking
Follow patients across time and care settings to understand disease progression, treatment patterns, and real-world outcomes.
Regulatory-Grade Data Quality
Our data governance processes support FDA 21 CFR Part 11, ICH E9, and other regulatory requirements for real-world evidence submissions.
Custom Cohort Analysis
Define your patient population with over 1,000 clinical attributes. Our data scientists can help build complex cohorts and run analyses.
How It Works

From research question
to actionable evidence

Our team works with you to design the study, extract the data, and deliver insights that meet your scientific and regulatory needs.

1
Define your research question

Our scientific consultants help you structure your RWE study design — patient population, exposure definition, outcomes, and confounders.

2
Data extraction and analysis

We query our 300M+ patient database to build your cohort, extract longitudinal data, and apply the statistical analyses your study requires.

3
Insights delivered

Receive structured datasets, summary tables, and visualizations. Our team provides regulatory consulting to support submissions if needed.

300M+
Unique patient records
40B+
Clinical data points
6,000+
Practice network sites
18mo → wks
Research timeline compression
Get Started

Ready to see what
Veradigm can do?

Join thousands using Veradigm to deliver smarter care.

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