TrialLens

TrialLens™ is a real-time clinical trial analytics platform developed by Clinical ink, designed to empower study teams with actionable insights across compliance, enrollment, device performance, and patient data. By centralizing critical trial intelligence into a powerful, intuitive analytics dashboard, TrialLens™ enables smarter decisions and supports faster, more efficient, and more compliant clinical trials.

TrialLens™ is built for clinical study teams seeking to elevate their oversight capabilities without requiring deep technical expertise. Its role-based access controls and self-service analytics tools make it accessible to a broad range of users, from site coordinators to data managers and clinical operations leaders.

Proactive Compliance Monitoring

• Provides real-time visibility into study adherence at the site, participant, and task level
• Features intuitive flagging, visual indicators, and trend analysis to surface compliance issues early
• Enables teams to identify and address non-compliance before it impacts study integrity or outcomes

Streamlined Operational Oversight

• Centralizes critical operational data including enrollment trends, device inventory, and sync status
• Helps study teams efficiently manage logistics and reduce delays across all trial sites
• Ensures data continuity by providing a unified view of field-to-server data flow

Enhanced Data Quality and Insights

• Integrates biomarker and patient diary review tools to support thorough data analysis
• Identifies anomalies, outliers, and abnormal patterns in both patient-reported and device-generated data
• Supports early detection of clinical signals and helps maintain high data quality throughout the trial

Empowered, Secure Access to Insights

• Combines role-based access control with Amazon Q-powered self-service analytics
• Allows users to explore their own data securely and intuitively using natural language queries
• Delivers visual and text-based responses, enabling flexible, on-demand insights beyond standard dashboard views without requiring technical expertise

Key Features

• Real-Time Study Adherence and Compliance Monitoring: Track participant and site compliance with visual indicators, flag tables, and trend analysis; instantly identify non-compliance at the task level and take corrective action
• Integrated Device and Data Sync Oversight: Monitor sync status of all study devices including data freshness, pending uploads, and inventory tracking, with proactive alerts to ensure seamless data flow
• Advanced Biomarker and Diary Data Review: Analyze raw and summarized biomarker data from connected devices and review patient diaries with filtering, sorting, and anomaly detection capabilities
• Self-Service Analytics with Amazon Q: Empower users to query their own data using natural language, receiving visual and text-based responses for flexible, on-demand insights

TrialLens™ is part of the broader Clinical ink ecosystem, which also encompasses eSource, eCOA, eConsent, patient engagement, telehealth, sensors and wearables, and digital biomarker solutions. The platform is designed to integrate within existing clinical trial workflows, supporting study teams in achieving greater operational efficiency and data integrity across all trial sites.