NCI's Clinical Trials Reporting Program
Introduction to NCI's new clinical trials reporting requirements.

Cancer Data Standards Repository (caDSR) for Common Data Elements
A repository of terms that medical providers may use to collect patient information for clinical trials or for cancer care. NCI hopes to facilitate uniform standards for cancer clinical trials and patient care by assembling and maintaining this information on-line for all interested caregivers.

NCI-CTEP: Clinical Data Update System
Primary data reporting mechanism for all NCI-sponsored clinical trials.

Adverse Event Expedited Reporting System
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 an NCI-sponsored investigational agent.

Common Toxicity Criteria and Common Terminology Criteria for Adverse Events
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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