September 30, 2024
Accelerate Trials
Clinion CTMS system is an integrated clinical trial management software that allows users real-time visibility across the study spectrum, allowing for real-time interventions and course correction, leading to accelerated study timelines.
Reduced Trial Costs
Customized workflows, pre-set processes, real-time status reports, automated alerts, real-time monitoring, holistic visibility – result in immediate and sustained efficiencies to reduce trial costs significantly.
Enhanced Visibility
Real-time Integration gives enhanced visibility into all aspects of the clinical research process - from study plan, design, site selection, subject recruitment, data capture, monitoring, remote monitoring, drug allotment, Inventory management and data management.
Feature-rich and Versatile
Clinion clinical trial management system (CTMS) manages a large part of clinical research operations. Moreover, it is constantly evolving, adding new features and modules almost daily, making it more versatile and user-friendly for its users.
Manage Clinical Trial Operations, Collaborate With Stakeholders And View Real-Time Data All At One Place With Clinion CTMS System
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Project Management
Project ManagementEnables study project managers to manage studies remotely by setting up milestones and assigning CRAs (Clinical Research Associates) to studies and sites.
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IP Inventory Management
IP Inventory ManagementEfficient inventory tracking right from receipt to issue to returns. Product expiry and inventory replenishment notifications in real-time. Auto and manual indent management.
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Robust Financial
Management
Robust Financial
ManagementOur dashboards and reports display milestones, payment receipts, expenses, dues and budgets that help monitor milestones and invoices alongside expenses entirely online.
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Advanced Dashboards
and Reporting
Advanced Dashboards
and ReportingImproved operational efficiency as our dashboards continuously monitor and display finances, projects, inventory and field results with effective reporting.
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Site Monitoring
Site MonitoringEnables Project Monitors and Clinical Research Associates (CRAs) to schedule monitoring visits across studies and CRAs to submit various monitoring reports approved by project managers.
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Document Management
Document ManagementManage all your study documents in one place so that they are accessible to both study and site personnel - Control who can access those documents and who cannot.
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Milestone Supervision
Milestone SupervisionEfficiently track and manage clinical trial milestones, ensuring timely protocol adherence and compliance. Streamline communication, enhance project visibility, and optimize trial timelines
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Task coordination
Task coordinationOptimize task allocation and monitoring in clinical trials, ensuring timely execution of study activities and protocol adherence. Streamline workflows, assign responsibilities, and track progress.
