Consumer Packaged Goods
Mobile Clinical Trial Management System
Benefits
Features
Electronic Data Capture
Remote patient monitoring leading to real-time data and real-world behavioral evidence to impact market access
Subject Verification for 155 Countries
No Borders: Expand your study participant reach globally
Electronic Clinical Outcomes Assessment & Patient Reported Outcomes
Respond to AE & SAE when they happen, during trials and the lifetime use of the product
Machine Learning and AI
Fully leverage the FDA’s adaptive design; course correct for dosage, population size and more
Comprehensive Bluetooth Device Integration
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
eCRF and Field CRF
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
Class-leading clinical standards and compliance
GCP, 21 CFR Part 11, HIPAA & GDPR Compliance
Payment Automation
Pay using PayPal
eConsent & eSignature
Expand the informed consent (eIC) needed based on real-time data insights
eAudits
Real-time data validation creates lifetime legal protections through data analytics, machine learning and AI
Behavioral Tools
For enhanced collection of Predictive, QOL and PRO data.
- Our unique behavioral recruitment engine qualifies potential participants based on behavioral assessments, to determine if a participant is a high-risk for withdrawal, protocol deviation or a potential superstar, and let’s get them enrolled.
- Imagine running a parallel study along with the primary study, for a secondary endpoint that identifies both positive and negative behaviors in relation to the IP.
- Imagine being able to track those behaviors, in tandem with machine learning, for the consumer's lifetime use of product.
