Clinical Trials Applications
The caBIG® program has built and configured the six applications listed below to work together to form a clinical trials management system known as the Clinical Trials Compatibility Framework. To learn more about each of the applications in the bundle click on the links below and if you like, follow those links into the caBIG® websites for additional details, examples, video demonstrations, and manuals. If you want to learn more about pricing and what is included click on teh subscribe button at the bottom of this page.
| Cancer Adverse Event Reporting System (caAERS) | Enables capture, management, querying and reporting of adverse events. |
| Cancer Central Clinical Participant Registry (C3PR) | Tracks subject registration and enrollment statistics for participants across studies, sites, systems, and organizations. |
| Cancer Data Exchange (caXchange) | Enables the translation of multiple source data formats into HL7 version 3 and the ability to automatically capture clinical laboratory data from laboratory systems and translate and import data into caBIG® compatible clinical trials databases. |
| Patient Study Calendar (PSC) | Enables trial managers to schedule and manage treatment and care activities for each participant in a clinical trial, ranging from epidemiological (and population) studies, observational studies, and interventional studies. PSC includes workflow, event-driven and date-driven tags and the ability to manage screening, registration, monitoring and long-term follow-up. |
| Clinical Trials Object Data System (CTODS) | Enables storing and sharing of clinical trials data in both identifiable and de-identified forms. Enables data from any Clinical Trials Data Management System (CDMS) or data source to be available to the research community |
To learn more about the Clinical Trial Compatibility Framework and see demos and overviews visit the caBIG® community website.
Clinical Trials Research
