Full cycle product for Research and Development teams in Pharmaceutical Industry. The product includes Electronic Trial Master File, Trial Management, Logistics and Inventory, Electronic Document Management with eSignature support. That is suitable for regulated areas as it is fully compliant with 21CFR Part 11 requirements.
Clinion - Clinical Trial Management Software (CTMS) gives enhanced visibility into all aspects of the clinical trial process - from study plan, Remote monitoring, and Clinical data management
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.
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