Octalsoft CTMS helps Lifesciences organizations in planning, tracking and reporting progress of a clinical trial. It helps research organizations by enabling process automation and ensuring regulatory compliance.
The CTMS solution from Octalsoft provides comprehensive clinical trial monitoring capability with patient visit tracker & integrated approval workflow of CRA visit monitoring reports. The action item or Issue management feature allows entry, tracking and reporting of regulatory and protocol compliance issues. Integrated IP Supply Management, Finance, and Project Management provide complete control and real-time insight into your clinical trial process.
Product Overview
Octalsoft CTMS provides a centralized database for clinical trial team including Sponsors, CROs and Investigators
Octalsoft CTMS provides clinical trial stakeholders with relevant and timely information
Consistent clinical trial data available at finger tips enables proactive management and allows sponsor and clinical research organization to take critical decisions timely and accurately
Octalsoft CTMS provides clinical trial monitoring and project management tools to clinical research associates and managers
Gain valuable insight in sites progress with subject enrollment and progression through the study. Subject calendar helps site coordinators track subject visits proactively
With Octalsoft CTMS, manage your trial budget effectively and track your budget overrun
Octalsoft CTMS enhances process compliance by enabling automation in generating and submitting site visit reports and tracking and managing deviations
Octalsoft CTMS automates investigator payment and enables improved control over process by integrating required workflow in processing payments to sites and investigators
A single source of real-time clinical trial database facilitates collaboration among study team members
Product Benefits
Streamlined and standardized processes results in immediate efficiencies for clinical operations
Ability to assign targets to sites and track progress in real time results in identifying and recruiting high performing sites thus resulting in faster subject enrollment.
Automate investigator and vendor payments based on pre-agreed milestones
Automation in generating visit reports, tracking deviations, and centralized real time access to study data reduces administrative burden and increased capacity for the clinical research team
Reduction in redundant system and processes shortens the entire clinical trial lifecycle
