Monitor Clinical Trial Sites in Real Time—From Anywhere
ResearchPRO gives you centralized access to real-time site data, audit trails, and query management tools—so you can stay on track, reduce errors, and run more efficient studies.
Remote monitoring
Incomplete and inaccurate data sets can impede study success, resulting in over-enrollments, incorrect conclusions, and unanswered questions.
With PatientIQ you gain:
Real-time access to data anywhere
Advanced data monitoring functionality
Enhanced compliance, data quality and integrity
Electronic case report forms (eCRF)
Complex forms and poor user experience can lead to incomplete and inaccurate data
With PatientIQ you gain:
User-friendly custom form builder
Advanced conditional logic simplifying form completion
Ability to embed custom eCRFs in the EHR]
Electronic informed consent (eConsent)
Traditional paper consent forms are outdated and ineffective, causing disruptions to clinical workflows.
With PatientIQ you gain:
In-clinic and mobile friendly eConsent workflows
21 CFR Part 11 compliant module
Intuitive and user-friendly digital form management
Electronic patient-reported outcomes (ePRO)
Inefficient and manual processes impede the ability to collect crucial patient-reported data at scale.
With PatientIQ you gain:
EHR-integrated patient enrollment
Automated, web-based engagement for easy patient access
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Industry-leading outcomes workflows and analytics
Reporting & analytics
Lack of funding, time, and expertise can limit the quality of data analysis, which leads to rushed processes and reliance on simpler methods, compromising the depth of analysis.
With PatientIQ you gain:
Proprietary analytics engine
Advanced data modeling and visualizations
Automated statistical analysis to uncover significant findings.
