Trialize AG provides a Clinical Trial Operating System that integrates EDC, eCOA/ePRO, eConsent, TeleVisits, RTSM, medical coding and lab modules with automation and analytics for study operations. The platform automates study build (protocol → CRFs), query handling, coding and real‑time monitoring and includes predictive models and AI‑assisted workflows.
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Industry:Research & DevelopmentSoftware Development
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EDC, eCOA/ePRO, eConsent, TeleVisits, RTSM, Medical Coding and Labs as integrated modules for study design, data capture, monitoring and operational control.
AI Ops for Clinical Trials
AI-powered operations layer for recruitment, risk-based monitoring, data cleaning, forecasting and adaptive designs with live visibility across studies and risks.
Study setup and protocol-to-CRF automation
Upload of protocols, automatic creation of validated database structures, CRFs, edit checks and validation rules for a fast study start.
Recruitment and pre-screening of study participants
NLP- and rule-based eligibility assessment, virtual preselection, multi-channel invitations and remote consent for faster recruitment of suitable participants.
Electronic consent and ePRO/eCOA
Remote consent, biometric and face-scan signature, patient-centric capture of outcomes, diaries and treatment data via digital channels.
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