Clinical Trial Application Bundle

 Hosted caBIG® Application Bundles 

 

Subscribe to one of our monthly packages now and you will have the ability to use hosted caBIG® applications today. No need to install any software. Our hosting service is simple, reliable, and hassle free.

caBIG® Application Bundles. Our SaaS hosting model makes using these outstanding software packages easy and hassle free. When we receive your order we will commission a fully configured dedicated virtual server with your selected caBIG® application installed and ready to use.

What is it? This is subscription-based web access to the caBIG® Clinical Trials Compatibility Framework (CTCF) for a fixed monthly fee. There are six applications that collectively function as a clinical trial management system that includes patient scheduling and adverse event reporting in addition to data repositories.

Who is it for? Our standard configuration of this software is designed for a group that wants to use the caBIG® to support a trial but who may not want to own and operate the required infrastructure. It is particularily useful for multi-site or multi-institute studies where the data and associated systems can reside with a trusted third party. As your needs grow we will scale the infrastructure to support your requirements. For an overview of how our Software-as-a-Service (SaaS) model works click here.
 

If you are a large organization or are planning a large or complex trial that has specific information technology requirements contact us and our engineers will help you size your initial system.

For additional information on what is provided ? Click Here.
 

caBIG® Clinical Trials Compatibility Framework (CTCF) Bundle: A Clinical Trials Management Solution

Today we offer the caBIG® Clinical Trials Compatibility Framework (CTCF) Bundle which facilitates electronic clinical research data management and enables the comprehensive sharing and integration of information. Specifically, the application bundle contains the caBIG® Clinical Trials Suite, which supports the management of study participant information through the clinical trial lifecycle. The CTCF framework also connects software tools to existing data management systems and to the caBIG® infrastructure.

The CTCF consists of five applications that are bundled together and designed to interoperate and support the work flow typically found during the execution of clinical trials. The suite enables the management of such common tasks as screening and patient accrual, scheduling and tracking patient actions during the trial, integrating laboratory results with the patient’s records, tracking and managing adverse events, and capturing, storing and analyzing trial data. These functions are accomplished through the use of five interoperable applications in conjunction with the caGrid infrastructure. The applications include:

  • Adverse event management [Cancer Adverse Event Reporting System (caAERS)]
  • Clinical data exchange [Cancer Data Exchange system (caXchange)]
  • Study participant calendar [Patient Study Calendar (PSC)]
  • Study participant registry [Cancer Central Clinical Participant Registry (C3PR)]
  • Clinical data repository [Clinical Trials Object Data System (CTODS)]

These applications, in combination with the core infrastructure functionality provided by caGrid and the Data Sharing & Security Framework, provide a clinical trial management system capable of supporting geographically distributed operations. For detailed information on each of the applications in the bundle click here.