Patient Data Reporting Solutions
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Democratizing Clinical Research With Castor
5/11/2023
Execute your study with Castor using modular solutions or as a platform package.
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Medable eCOA
5/26/2022
Medable eCOA is designed to enhance your decentralized trial capabilities with all features native to the platform. Modular by design, use what you need, not what you don’t.
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Your Medical Imaging Workflow Solution
2/2/2026
By addressing common "pain points" such as the complex handling of DICOM files and unreliable transfer methods, the Judi platform prevents workflows from coming to a grinding halt.
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Bridging The Gap Between EHR And EDC
5/19/2025
Clinical trial sites have long relied on manual, error-prone processes to transfer patient data from EHRs into EDC systems, but integrated solutions make streamlining this workflow quick and simple.
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A New Digital Health Solution For Long-Term Cough Monitoring
4/15/2025
Discover how our innovative solution transforms cough measurement — providing accurate, objective insights to enhance treatment, detect exacerbations early, and improve patient outcomes.
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Streamline Your Regulatory Process
1/18/2022
The Advarra eRegulatory Management System (Advarra eReg) provides integrated protocol, staff, and institution documentation to streamline regulatory process and enhance compliance.
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Clinical Data Studio: Unlock The True Power Of Clinical Trial Data
1/5/2026
Experience a transformative AI-powered data quality management solution that unifies study teams by providing seamless access to data from all clinical data sources.
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Accelerate Study Startup Through Better Collaboration
3/3/2025
With 80% of trials failing to enroll patients on time, improved collaboration between sites and sponsors is essential.
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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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Explore Medable Studio
9/23/2024
Achieve unprecedented control over the study creation and deployment process with a no-code interface.