Mobile Clinical Trial Management System
Remote patient monitoring leading to real-time data and real-world behavioral evidence to impact market access
No Borders: Expand your study participant reach globally
Respond to AE & SAE when they happen, during trials and the lifetime use of the product
Fully leverage the FDA’s adaptive design; course correct for dosage, population size and more
Empowers “Bring Your Own Device” and the data collection that’s expanded and enabled – benefitting from every connected device and applications’ data directly into your subjects’ data capture
Enables “hybrid studies” with high-touch eVisits via eCRF, web & mobile
Either eliminate or reduce your CRO brick & mortar costs; increase ROI for dollars already invested in the CRO by expanding reach, touch and frequency of interaction
GCP, 21 CFR Part 11, HIPAA & GDPR Compliance
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Expand the informed consent (eIC) needed based on real-time data insights
Real-time data validation creates lifetime legal protections through data analytics, machine learning and AI