ResearchPRO
Clinical Research Software That Scales With You
Accelerate study timelines with built-in ePROs, eConsent, EDC, and real-time analytics.
Book a Demo and Streamline Your Next Study
Why ResearchPRO?
Clinical research demands scalability, speed, and precision. ResearchPRO is the clinical research software built for modern trials.
Accurate & Automated Trial Data
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Ensure 21 CFR Part 11 compliance with secure data capture
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Automate ePRO workflows and reduce site burden
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Capture validated outcomes at scale across study arms
Real-Time Research Insights
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Visualize trial trends and site performance instantly
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Validate and clean data in real time
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Make evidence-based study decisions faster
Streamline Clinical Trial Efficiency
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Launch studies quickly with flexible EDC tools
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Standardize data capture across study sites
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Reduce manual data entry and reporting delays
ePROs for Clinical Trials
Deploy scalable patient-reported outcome measures that drive trial efficiency, data accuracy, and patient experience—backed by real-time analytics and site-level tracking.

Real-Time Monitoring & Analytics
Gain clinical research insights on study performance, patient-reported data, and compliance across all trial phases.

Simple Patient Experience, High Compliance
The PatientIQ platform is built to support your brand and patient relationships, featuring frictionless login, white-labeled patient engagement, and access across all devices.


Frictionless
login

Access on
all devices

Automated
reminders

White-labeled
engagement

Clear task
assignment
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