Clinical Trial management system (CTMS) | clinical trial software| Clinion CTMS

Clinion CTMS Software provides an integrated, comprehensive solution for Clinical trial management.It is an essential set of tools to effectively plan, monitor and track your clinical study portfolio

Accelerate Trials

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.

Enhanced Visibility

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.

Enables study project managers to manage studies remotely by setting up milestones and assigning CRAs (Clinical Research Associates) to studies and sites.

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.

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

Enables Project Monitors and CRAs to schedule monitoring visits across studies and CRAs to submit various monitoring reports approved by project managers.

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.

Clinion is an integrated eClinical Platform consisting of an Electronic Data Capture (EDC), Randomisation and Trial Supply Management (IWRS/RTSM), Patient Reported Outcomes (eCOA) and Clinical Trial Management Systems (CTMS).

Clinion IT Services is a technology company offering innovative software solutions in the life sciences and pharmaceutical industries since 2010. Our first product, Clinion is an integrated clinical trial solution for small and medium CROs, academic research organizations and pharmaceutical companies.

Our Vision

We envisage Clinion to be the integrated eClinical platform of choice for small and medium CROs, and academic and pharmaceutical organisations in the global market.

Our Story Clinion is an integrated eClinical Platform consisting of an Electronic Data Capture (Edc), Randomisation and Trial Supply Management (Iwrs/Rtsm), Patient Reported Outcomes (ePro) and Clinical Trial Management Systems (Ctms).