From Phase I trials to global real-world studies, we support every stage of the clinical research journey with a patient-centric approach. Our solutions harness real-world data in real time to accelerate innovation and unlock value across the drug development lifecycle.
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Remote Patient Monitoring in your Phase I-II trials: Patient-centricity driving faster, safer & more efficient oncology trials.
Design patient-centric programs that boost experience, adherence, and outcomes — while generating real-world, patient-driven insights.
Accelerate and de-risk HTA submissions, label expansion, price negotiations, and post-marketing studies by transforming fragmented clinical and patient data into regulatory-grade real-world evidence.
Cutting-edge digital tools designed specifically for life sciences
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Real-time tracking of patient-reported symptoms and adverse events with automated safety alerts
Patient-facing mobile apps for tracking symptoms, ePROS & QoL, with timely content delivery
Advanced structuring of clinical and biological data for improved patient stratification
Real-world analysis of treatment outcomes to support market access and value demonstration
Intuitive dashboards for data-driven decision-making in clinical and commercial operations
Secure access to aggregated insights from 120+ institutions and 100,000+ oncology patients by end of 2026
Powered by advanced analytics, we collect QoL and PRO-CTCAE (symptoms/toxicity) data in routine setting
Our platform connects patients, care teams, and researchers—enabling the seamless and consistent capture of structured real-world data
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Embedded in routine care across 120+ sites and 20,000 patients, our solution leverages real-world data to deliver valuable clinical insights
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Turning fragmented clinical and patient-reported information into actionable insights for clinical research, market access, and publications
Check their availability and book a meeting through their event calendars.
Book a virtual meeting anytime with our team.
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