Clinical Technologies Solutions
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Unified Clinical Trial Platform Delivering Patient, Data, And Study Experiences
2/3/2026
See how AI- and automation-powered experiences are replacing manual, disconnected systems to improve patient engagement, enhance data quality, and optimize study design.
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The Definitive Infrastructure For Modern Drug Development
4/9/2026
Modernize clinical trials with AI-powered recruitment and automated EHR data capture to accelerate enrollment, improve data quality, and expand patient access across a global research network.
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Enable Value-Based Evaluation Of Medicines
3/28/2025
Trial@home, CHDR’s dedicated strategy for off-site clinical trials, enables investigators to collect information as trial participants go about their day to day activities.
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Generate Regulatory-Grade, RWE With Speed And Efficiency
11/21/2025
For teams managing real-world evidence or post-market studies, automation offers a scalable solution to streamline workflows, maintain compliance, and accelerate decision-making.
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Rave Lite For Phase IV Trials
1/13/2025
Designed for post-marketing surveillance and observational studies, Medidata’s Rave EDC offers a tailored and scalable solution for Phase IV and late-stage trials.
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Elosity Overview
4/21/2026
Clinical trials evolve fast. Flexible RTSM with automation, continuous updates, and clear visibility helps teams handle complexity, speed amendments, and stay in control globally.
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Greenphire Patient Payments
10/24/2025
esigned for sponsors, CROs, sites, and patients, this modern solution delivers real-time data that supports crucial decisions during investigator grant budgeting, randomization, patient payments, and endpoint collection.
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Securely Archive And Lock Down Your eTMF While Providing Inspector Access And Ensuring Ongoing Compliance
3/14/2023
Trying to archive a TMF delivered by a CRO? Need out of non-compliant file systems? Interested in reducing archival costs? Discover how IQVIA eArchive could be the solution for these issues and more.
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Synthetic Control ArmĀ®: The Smart External Control Arm Solution
7/21/2025
Discover how an external control arm can help you generate rigorous evidence, accelerate decisions, and keep your trial on track when a concurrent control isn’t feasible.
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IQVIA Safety Notifications
5/20/2020
Now featuring cross-trial functionality, IQVIA Safety Notifications gives sponsors and contract research organizations (CROs) a centralized, simple solution for disseminating, managing, and tracking SUSARs and other safety notifications.