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Clinion CTMS – clinion Request Demo

clinion

Plan, Manage and Track
Your Studies at One Place

An Integrated Clinical Trial Management System (CTMS) That
Gives CROs And Sponsors Greater Control And Visibility

Accelerate Trials

Clinion CTMS is an integrated clinical trial management system 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 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

Study Setup

Project Management

Project 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 Management

IP 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.

Robust Financial
Management

Robust Financial
Management



Our dashboards and reports display milestones, payment receipts, expenses, dues and budgets that help monitor milestones and invoices alongside expenses entirely online.

Advanced Dashboards
and Reporting

Visit Scheduler



Improved operational efficiency as our dashboards continuously monitor and display finances, projects, inventory and field results with effective reporting.

Site Monitoring

Site Monitoring



Enables Project Monitors and Clinical Research Associates (CRAs) to schedule monitoring visits across studies and CRAs to submit various monitoring reports approved by project managers.

Document Management

Document 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.

Milestone Supervision

Milestone Supervision



Efficiently track and manage clinical trial milestones, ensuring timely protocol adherence and compliance. Streamline communication, enhance project visibility, and optimize trial timelines

Task coordination

Task coordination



Optimize task allocation and monitoring in clinical trials, ensuring timely execution of study activities and protocol adherence. Streamline workflows, assign responsibilities, and track progress.

See How Our Clinical Trial Management System (CTMS) Helps You
Gain Complete Control Over Clinical Operations!