CLINICAL TRIAL DASHBOARD
Real-Time Analytics Keep Studies On Track
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TranSenda's Clinical Trial Dashboard™ gives you the insight you need to assume greater control of your studies. As an extension of TranSenda's Clinical Trial Manager™, the Dashboard aggregates real-time study data into intuitive views of the most essential performance metrics for sites and studies. |
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Dashboard lets you view the actual progress and milestones of every study and site—alongside your projections—so you're the first to know if a study or site is falling behind. Intuitive access to such meaningful data allows proactive controls throughout study performance. For example, if an entire study is lagging, the CFO can forecast the delay's impact on the overall budget.
The result is the business agility entrepreneurial sponsors, CROs and blended organizations need to stay competitive. Best of all, the data driving TranSenda's Dashboard is a value-added byproduct of Clinical Trial Manager—extending the value of the industry's most agile and affordable clinical trial performance system.
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Benefits
- Quickly review essential performance metrics by study and/or site breakdown
- Monitor your study's actual progress against projections
- Control risk by predicting, assessing and avoiding delays and costs
- Assess your best performing sites to support future study decisions
Features
- Essential view of study-by-study actual vs. projected accrual metrics, subject accrual performance and study milestones
- Intuitive overview of specific site metrics across all sites for a single study, including site status pie chart, site list table and subject enrollment status
- CTMS integration extends user permissions through Dashboard, ensuring users only access relevant study/site data
Technology Overview
Web-Based Technology
TranSenda's modular applications are web-enabled by design, providing secure, flexible universal access for all users regardless of their locations, and eliminating the administrative headaches of installing and updating software on multiple workstations.
Integration Capabilities
TranSenda's open standards architecture, based upon Microsoft's .NET technology, allows our applications to integrate with legacy systems and other solutions in the TranSenda Central system of integrated, modular clinical trial applications. The platform allows for the exchange and presentation of data from multiple systems to internal and external users in real-time utilizing industry standards such as CDISC or other XML-based conventions. Maximum interoperability is maintained through links to outside third-party applications or databases for complete end-to-end trial management.
The Platform
Because all solutions are built upon TranSenda's Clinical Trial Process Platform, TranSenda's proprietary process-based platform, the solutions inherit characteristics that impart extraordinary manageability and maximum scalability. By utilizing applications built upon the platform, business logic and workflow can be applied to create universal exchange and presentation of data from multiple systems to internal users and sponsors in real-time. Our no-code-required™ technology enables unprecedented process control, allowing efficient creation and modification of workflow to remain in compliance with business and regulatory requirements. In addition, the platform supports 21 CFR Part 11 compliance for all TranSenda applications.
Hosting Services
If you have limited IT resources or wish to minimize your infrastructure investment in order to simplify system management, TranSenda offers hosting services for all applications.







