Octalsoft CTMS enables global CROs maintain a centralized clinical trial database providing users with the most relevant and up to date information based on their specific roles & responsibilities. Extending the visibility thus, the Clinical Trial Management System Software ensures increased efficiency & quicker operations.
The Clinical research software solution from Octalsoft provides comprehensive clinical trial monitoring software solution 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.
Octalsoft CTMS provides a centralized database for clinical trial team including Sponsors, CROs and Investigators
Prompt Access to Data
Octalsoft CTMS provides clinical trial stakeholders with relevant and timely information
Facilitates Decision Making
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
Better Trial results
Streamlined and standardized processes results in immediate efficiencies for clinical operations
Faster Subject Enrollment
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.
Improved Investigator relationships
Automate investigator and vendor payments based on pre-agreed milestones
Increased clinical research associate productivity
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
Lower Trial costs
Reduction in redundant system and processes shortens the entire clinical trial lifecycle