Patient-Reported Outcomes, Reimagined for Modern Trials
Capture real-time data from anywhere — safely, simply, and at scale with our intuitive, patient-friendly ePRO/eCOA solutions.
A Critical Foundation for Decentralized, Patient-Centric Trials
Modern clinical trials demand modern tools for capturing the patient voice — wherever they are.
Patients report from home or during daily life, increasing compliance and data quality.
Capture complex assessments digitally with validated instruments and scales.
eConsent, visit reminders, and outcomes in one seamless patient experience.
"Studies using ePRO report 3–5x higher compliance compared to paper methods."See Compliance Impact Blog
AI-Powered eCOA, From Protocol to Production
Mahalo's AI engine transforms your protocol into ready-to-deploy eCOA forms in minutes, not weeks.
- Upload trial protocol → AI parses visit schedule + assessments
- Auto-generates eCOA screens + logic
- Suggests validated instruments
- Translates forms, tests logic, prepares for deployment
Everything You Need to Capture the Full Patient Voice
Comprehensive tools designed for modern clinical trials and real-world evidence generation.
Support for 50+ languages with automated translation workflows.
Instant notifications for sites and sponsors on critical data points.
BYOD or site-provided devices with online/offline capabilities.
Seamless flow from consent to outcomes collection.
AI-powered adherence reminders and visit planning.
Automatic data flow to EDC and analytics dashboards.
Proven Across Patient-Reported Trials
Specialized solutions for every therapeutic area, with validated instruments and custom workflows.
Flexible by Design — Remote or On-Site
Whether your trial is fully decentralized, hybrid, or traditional site-based, Mahalo ePRO adapts to your needs.
- Virtual visits with integrated video
- Home-based assessments and diaries
- Wearable device integration
- BYOD with offline capabilities
- Caregiver proxy reporting options
Built for Global Trials and Regulatory Confidence
Enterprise-grade security and compliance, with patient-friendly design.
FDA eCOA Guidance Aligned
Fully compliant with FDA guidance on electronic clinical outcome assessments.
21 CFR Part 11 + GDPR
Electronic records and signatures meet global regulatory requirements.
In-app Patient Help & Alerts
Real-time support and guidance for participants when they need it.
AI-Validated Form Logic
Intelligent validation ensures data integrity and reduces errors.
Multimedia eConsent Integration
Seamless flow from informed consent to outcomes collection.
Complete Audit Trail
Comprehensive tracking of all system interactions and data changes.
How Mahalo Compares
See how our AI-powered ePRO/eCOA solution stacks up against traditional platforms.
Mahalo | Medidata | Medable | |
|---|---|---|---|
| Setup Time | Days | Weeks to Months | Weeks |
| AI-Powered Form Generation | Yes | No | Limited |
| Translation Automation | Full AI + Human Review | Manual Process | Semi-Automated |
| Mid-Study Changes | Self-Service | Vendor Support Required | Limited Self-Service |
| DCT-Native Design | Yes | Add-on | Yes |
Launch in 10 Days: Your ePRO Setup Plan
Get your ePRO solution up and running quickly with our proven implementation methodology.
Day 1-2
Protocol Analysis & Form Design
Day 3-4
eCOA Build & Logic Implementation
Day 5-6
Testing & Validation
Day 7-8
Translation & Localization
Day 9-10
Training & Go-Live
Trusted in High-Stakes Trials
See how leading research teams are using Mahalo ePRO/eCOA to transform their studies.
FAQs About Mahalo ePRO & eCOA
Common questions about our platform, capabilities, and implementation.
Modern Trials Need Modern Tools
Capture the full patient voice — faster, smarter, and with confidence using Mahalo's AI-powered ePRO & eCOA platform.