CCTS

From CTMS_WIKI

Background

The caBIG Clinical Trials Suite (CCTS) is an enterprise clinical trials system being designed primarily for use in trial sites. The suite is comprised of a collection of interoperable modules covering a broad range of key areas in cancer clinical trials management. These include patient registration via C3PR, patient scheduling via PSC, adverse events reporting via caAERS, lab analysis via LabViewer, and clinical data management via C3D. Integration between these applications is centered around five key scenarios: Study Creation, Register Subject, Load Labs in CDMS, Lab-driven AE Creation, and AE-Triggered Schedule Change. The implementation is based upon the caGrid infrastructure with caXchange as the Enterprise Service Bus for reliable message routing and GAARDS providing robust security.

Documentation

CCTS 1.1 Documentation

CCTS 2.0 Documentation

Team

Planning

The CCTS Team is currently working on the developement and release of CCTS 1.1. The target release date is October 31.

Meetings

Daily Scrum

• Everyday, 4:00-4:15 EST
• Teleconference: 1-800- 857-4816
• Passcode: 85670
• Web Centra: http://ncicb.centra.com
• Meeting ID: CTMS Suite

Templates

CCTS 2.0 Templates

• Template:CCTS Background
• Template:CCTS Team
• Template:CCTS Documentation
• Template:CCTS Scope Disclaimer
• Template:CCTS Use Case Summary
• Template:CCTS Application Summary

CCTS 1.1 Templates

• Template:CCTS 1.1 Background
• Template:CCTS 1.1 Team
• Template:CCTS 1.1 Documentation
• Template:CCTS 1.1 Application Summary
• Template:CCTS 1.1 Roles