Tired of confusing Excel spreadsheets, email exchanges, and endlessly searching for crucial updates, critical files or the latest financial data? TrialPoint™ CTMS makes it easy to manage your study in a single secure online location.
The system provides…
- single data repository for administrative, operational and financial data
- anytime, anywhere access to your study on any device
- custom dashboards for critical endpoint metrics
- business analytics and much more...
ResultStreamline your workflow in a just a few clicks. No matter where you are, or what time it is, TrialPoint™ CTMS keeps you connected to the rest of your team – optimizing productivity and keeping all study activities fast and transparent.
TrialPoint™ EDC is easy to configure, easy to use, and the coordinators love it. Our data managers are experts in converting clinical protocols into geek speak (metadata dictionaries for those in the know) and will configure TrialPoint™ to work for you; not against you. The system can accept any randomization string, media upload, or coding dictionary, it can even blind users to treatment assignments. To promote time-sensitive data collection the system will prospectively calculate visit windows and send out alerts and reminders keeping the team focused and on task.
Expert configuration and prospective e-monitoring tools lead to cleaner data, lower on-site monitoring costs, and earlier database closure
Often, the most time consuming and frustrating part of clinical research is keeping track of investigational product. With TrialPoint™ CSM you can record the shipping, use, and return of drugs, devices, and clinical supplies. This module integrates seamlessly with the EDC system to provide comprehensive real-time reporting on all inventories -- which makes it ideal for global Sponsors with large product lines and single product companies constantly shifting low inventory.
Real-time clinical supply reports promote compliance, reduce costs, and can prevent overproduction of investigational products
Nowadays, patient reported health outcomes and quality of life questionnaires are included in most trial designs and are responsible for many protocol compliance issues. Take a look at TrialPoint’s electronic Patient Reported Outcomes (ePRO) module which can be configured to fit any quality of life questionnaire or patient diary. This secure patient portal can be accessed remotely (even on a mobile device), can prompt patients to enter information within a defined window, and can automatically score the instruments providing you with analysis-ready data.
ePRO minimizes transcription errors, improves protocol compliance, and increases patient engagement and overall satisfaction.
Keeping track of external data generated during a trial is time consuming, confusing and prone to data loss. To avoid processing, shipping and tracking hundreds of media files we use TrialPoint’s Core Lab Integration module. This module accepts media uploads from sites, labels and stores the files, notifies the “readers” they have work to do, and automatically generates a subject specific core lab form for completion.
Core lab integration provides a single data repository for all research related data. The sites love it, the readers love it, and our Sponsors save time and money.
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