CLINICAL TRIAL MANAGER
Take Control of Your Clinical Trials
For emerging sponsors, biotech's and CROs who want to move beyond spreadsheets or who are avoiding software systems designed for large pharmaceuticals, TranSenda delivers a modular clinical trial management system (CTMS) that is specifically targeted to your unique needs. |
Product Sheet |
Designed with the versatility to accommodate your SOPs, Clinical Trial
Manager™ and its modularity deliver unparalleled flexibility and ease of use. After a few hours of training, your clinical professionals will be setting up studies, defining protocols, managing user permissions — without the aid of IT staff. As part of the TranSenda Central® system of integrated, modular clinical trial applications, all study data and protocols are extended and supported throughout complementary applications like Clinical Payment Manager™.
Whether managing multiple trials internally, or strategically outsourcing specific activities, TranSenda's modular Clinical Trial Manager is the ideal management system to allow emerging organizations to take control of the end-to-end clinical trial process. |
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Benefits
- Remote user access portals for all study team members, providing a single source for maintaining critical study data and documents and reducing the need for internal staff to input data
- Easy to setup using template-based study configuration wizard
- Users can securely perform study-specific roles via flexible operational permissions
- Facilitate system validation through embedded features, test scripts and documentation
Features
- Configurable for either single or multi-sponsor users
- Integrated contact management and messaging
- Robust scheduling functionality—sets multi-mode alert schedules and triggers
- Schedules, tracks and monitors patient visits and CRF receipts
- Track SAE disposition and reconciliation
- Advanced record lookup capability
- Template-based adjustable study configuration
- Dynamic site initiation
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.
