Clinical Trials Reporting Program
(Posted: 04/24/2009) - Information about NCI's new Clinical Trials Reporting Program (CTRP). The site is designed to guide clinical trial investigators and their staff through the process of registering trials with CTRP.

Cancer Data Standards Registry and Repository
The caDSR is a database and a set of application programming interfaces and tools used to create, edit, control, deploy, and find common data elements.

Clinical Data Update System (CDUS)
Primary data reporting mechanism for all NCI-sponsored clinical trials.

Adverse Event Expedited Reporting System (AdEERS)
NCI's Web-based system for submitting expedited reports for serious and/or unexpected events forwarded to designated recipients and the NCI for all trials using NCI-sponsored investigational agents.

Common Terminology Criteria for Adverse Events and Common Toxicity Criteria
Resources for standard terminology used to name and to describe the severity (grade) of adverse events that occur in the treatment of cancer.

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