Clinical Trial Management System
Electronic Data Capture
Interactive Web Response System
Agentic AI capabilities to power clinical trials
Remote Source Data Verification
Electronic Patient Reported Outcome
Electronic Informed Consent Form
Medical Imaging
Electronic Document Management System
Electronic Trial Master File
Clinical Trial Supply Management
Quality Management System
Warehouse Management System
Portfolio & Project Management System
Learning Management System
Laboratory Information Management System
Biorepository Management System
Hospital Information Management System
We accelerate, scale, eliminate risks, and improve trial outcomes for business success
We assist sites in bringing treatments and devices to patients sooner.
A comprehensive research technology platform to augment CRO efficiency
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A collection of insights, updates, and glimpses into the future
Browse our eClinical insights and fact sheets.
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Our origins: From an idea to eClinical excellence
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As you know, an EDC in clinical trials is a system for collecting, maintaining, and processing site-, patient-, and lab-reported data in an electronic format...
eConsent plays a vital role in enhancing existing clinical trials, but implementation teams continue to be concerned about the intricacies of eConsent acceptance in the...
What good is data that isn’t statistically solid, legible, and dependable? Not any good at all. With clinical data management, however, you can rest assured...
Humans, like the diseases and disorders they suffer from, are biologically complex. As a result, as scientists gain a better understanding of the body’s systems,...
The shift to more decentralized trials in response to COVID-19 pandemic constraints has shown that the clinical trial industry is capable of embracing new technologies...
An IRT system is known by several names, including IVRS, IWRS, IXRS, and RTSM, but regardless of its name, the system provides a comprehensive set...
Be part of a team that's breaking new ground and pushing the boundaries of what's possible.
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