Clinion CTMS 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.
Real-time Integration gives enhanced visibility into all aspects of the clinical trial 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 CTMS Software manages a large part of clinical trial 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.
Project ManagementProject Management
Enables study project managers to manage studies remotely by setting up milestones and assigning CRAs (Clinical Research Associates) to studies and sites.
IP Inventory ManagementIP Inventory Management
Efficient inventory tracking right from receipt to issue to returns. Product expiry and inventory replenishment notifications in real-time. Auto and manual indent management.
Our dashboards and reports display milestones, payment receipts, expenses, dues and budgets that help monitor milestones and invoices alongside expenses entirely online.
and ReportingAdvanced Dashboards
Improved operational efficiency as our dashboards continuously monitor and display finances, projects, inventory and field results with effective reporting.
Site MonitoringSite Monitoring
Enables Project Monitors and CRAs to schedule monitoring visits across studies and CRAs to submit various monitoring reports approved by project managers.
Document ManagementDocument Management
Manage 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.