National Cancer Institute   U.S. National Institutes of Health www.cancer.gov
caBIG® Knowledge Center: A part of the Enterprise Support Network

Template:Products

From CTMS_WIKI

Jump to: navigation, search

Contents

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 four key scenarios: Study Creation, Register Subject, Load Labs in CDMS, 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.

Cancer Adverse Events Reporting System (caAERS)

The Cancer Adverse Event Reporting System (caAERS) is an open source, standards-based, web application for documenting, managing, reporting, and analyzing adverse events (AEs). The system operates as both a repository for capturing and tracking routine and serious AEs and as a tool for preparing and submitting expedited AE reports to regulatory agencies.

End User Forum Developer Forum Releases Development Site Bug/Feature Tracker Code Base

Cancer Center Participant Registry (C3PR)

The Cancer Center Participant Registry (C3PR) is a web-based application used for end-to-end registration of patients to clinical trials including capturing the consent signed date, eligibility criteria, stratification, randomization, and screening, as well as coordinating multi-site clinical trial registration.

End User Forum Developer Forum Releases Development Site Bug/Feature Tracker Code Base

Patient Study Calendar (PSC)

A software product for creating and editing study calendar templates, tracking patient activities as they occur, and managing patient calendars during the conduct of a study.

End User Forum Developer Forum Releases Development Site Bug/Feature Tracker Code Base

LabViewer

Lab Viewer is a web based application developed by leveraging the SDK generated APIs of the CTODS Lab Domain UML model. Lab Viewer allows users to view laboratory activities that are stored in the CTODS Lab Domain database. Users are allowed to search the laboratory activity records by Patient Id, Study Id, Lab Start Date, and Lab End Date. Lab Viewer also allows users to send lab data in the form of XML messages via caXchange. The message type that can be sent is a Load Lab Data message to the local CDMS application (C3D) application.

End User Forum Developer Forum Releases [Development Site] Bug/Feature Tracker Code Base

C3D Connector

A service wrapper for C3D, an NCI-supported Clinical Data Management System.

End User Forum Developer Forum Releases Development Site Bug/Feature Tracker Code Base

caXchange

Central hub for exchanging clinical trials information and integrating caGrid-based services.

End User Forum Developer Forum Releases Development Site Bug/Feature Tracker Code Base
KC Projects