caBIG® has been partnering with regulatory bodies, pharmaceutical companies, the patient advocacy community, and organizations that design and run clinical trials to address the challenges of conducting clinical research.
In the aggregate, caBIG® tools—such as the ones mentioned below—comprise the building blocks of a system for end-to-end collection, management, and exchange of information from trial design and management through regulatory submission.
These caBIG® tools can help to mitigate unnecessary work delays, duplication of effort, human errors in data entry, and missed opportunities for data mining and secondary use of clinical trial data, as well as improve regulatory compliance.
Cancer Adverse Event Reporting System (caAERS)
The Cancer Adverse Event Reporting System (caAERS) captures and manages reports that describe adverse events that occur during clinical trials. Specifically, this tool:
- Allows local collection, management, and querying of adverse event data (both routine and serious)
- Supports regulatory compliances
The Patient Study Calendar developed by caBIG® enables clinical trial managers to schedule and manage treatment and care events for each participant in a clinical trial. Specifically, this tool:
- Represents already-existing workflows, processes, phases, and behaviors
- Allows easy management of the screening process, registration, monitoring, and follow-up with participants
- Accommodates multiple study design formats (population, observational, interventional, etc)
Complete caBIG® Clinical Trials Product Inventory
- Cancer Adverse Event Reporting System (caAERS) - Adverse event management
- Patient Study Calendar (PSC) - Study participant calendar
- Cancer Central Clinical Participant Registry (C3PR) - Study participant registry
- Cancer Data Exchange (caXchange) - Clinical data exchange
- Clinical Trials Object Data System (CTODS) - Virtual clinical data repository
- Cancer Central Clinical Database (C3D) - Clinical trials data management system
For a complete list of caBIG® tools, see our "Finding the Right Tools" section
Other caBIG® Links articles of interest to Clinical Research
C3PR: Enabling Cross-Institutional Clinical Trials Management
The Cancer Central Clinical Participant Registry streamlines the maintenance and use of patient information
Improving Efficiency of Clinical Trials with C3PR
The Cancer Central Clinical Participant Registry improves efficiency and accuracy in managing clinical trials participants at Georgetown University's Lombardi Comprehensive Cancer Center
Clinical Trials Management Software in Action at Duke University
The Cancer Central Clinical Database, an FDA-compliant clinical trial management platform, in action at Duke University Comprehensive Cancer Center
