ResearchPRO

ResearchPRO is an electronic data capture (EDC) platform developed by PatientIQ for clinical trials, registries, and outcomes-focused research. It is designed by in-house researchers and is backed by a network of clinical organizations and healthcare providers. The platform targets health systems, specialty practices, and medical device companies seeking to collect, manage, and analyze clinical research data more efficiently.

ResearchPRO aims to reduce the time and effort required to obtain actionable data by combining EHR integration, automated workflows, and a suite of research tools within a single platform.

Core EDC Modules

• Electronic Case Report Forms (eCRF): Includes a user-friendly custom form builder with advanced conditional logic to simplify form completion. eCRFs can be embedded directly within the EHR to reduce workflow disruption and improve data accuracy.
• Electronic Informed Consent (eConsent): Supports both in-clinic and mobile-friendly consent workflows. The module is 21 CFR Part 11 compliant and provides intuitive digital form management to replace paper-based consent processes.
• Electronic Patient-Reported Outcomes (ePRO): Offers EHR-integrated patient enrollment and automated, web-based patient engagement to facilitate collection of patient-reported data at scale. Includes outcomes workflows and analytics.
• Remote Monitoring: Provides real-time access to study data from any location, along with advanced data monitoring functionality to support compliance, data quality, and data integrity throughout a study.
• Reporting and Analytics: Features a proprietary analytics engine with advanced data modeling, visualizations, and automated statistical analysis to identify significant findings from collected data.

Platform Capabilities

• Scalable EHR integrations designed to work across departments for secure collection of patient-reported outcomes.
• Automated biostatistics engine, smart methods generator, and data visualizations for benchmarking patient populations and supporting quality reporting.
• Enterprise-grade security measures to protect patient health information and sensitive organizational data.
• Access to the PatientIQ network, a collaborative of healthcare organizations that share best practices, participate in registries, and conduct joint research.

Target User Groups

• Health systems: Supports scalable, EHR-integrated patient outcomes programs to advance care delivery.
• Specialty practices: Enables collection and use of patient outcomes data to demonstrate clinical performance.
• Medical device companies: Facilitates collection and analysis of clinical research data to validate and differentiate products.

ResearchPRO is built on the PatientIQ platform and supports compliance with 21 CFR Part 11 for electronic records and signatures. The platform is designed to integrate with existing EHR systems and has been used in scenarios such as migrating data from legacy EDC platforms and scaling clinical data collection across large health organizations.