ResearchPRO
Clinical research software that scales with you
Accelerate study timelines with built-in ePROs, eConsent, electronic data capture, 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
-
Ensure 21 CFR Part 11 compliance with secure data capture
-
Automate ePRO workflows and reduce site burden
-
Capture validated outcomes at scale across study arms
Real-time research insights
-
Visualize trial trends and site performance instantly
-
Validate and clean data in real time
-
Make evidence-based study decisions faster
Streamline clinical trial efficiency
-
Launch studies quickly with flexible EDC tools
-
Standardize data capture across study sites
-
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
Trusted by leading medical researchers
+0
Healthcare Organizations
+0
Healthcare providers
0M
Patients