The PRO Portal™ Platform is a rules-based system to automate PRO studies. It seamlessly integrates a virtual patient engagement channel with the physical workflow of clinicians, stakeholders, and partners. This robust platform supports:
- Fully-Configurable, Programmer-Free Customization per Study and Patient Subgroup
- Multiple Studies per Registry
- Dynamic Survey Engine with Triggers for Time and Events
- Event-Driven Diary
- Patient Self-Reported Information using any Validated or New Instrument
- Full Drug Dictionary & Symptom Library
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Secure Responsive Web Design for Full Device Independence
- Measures Symptoms, Medication Adherence, Comorbidities, & Other Complications
- Tracks Activities of Daily Living, Diet, Exercise, Physiologic Measures, Burden, & Impact
- Interactive, Real-Time Reporting of Portal Compliance and PRO, Clinical, & Claims Data
- Manages Adverse Events & Lab Results
- Automated, Customizable Alerts & Notifications for patients, providers, partners, and sponsors
