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Data Models for CTEP Systems
Request form to obtain models for use when configuring systems that will interact with CTEP applications
CTCAE (formerly known as CTC) v2.0 and v3.0
Standards used to grade, assign attribution and report side effects experienced by patients on clinical trials
Adverse Event Expedited Reporting System (AdEERS)
NCI's web-based system for submitting expedited report for serious and/or unexpected events to designated recipients and the NCI for all trials using a NCI-sponsored investigational agent (password protected: contact CTEP Help at info@ctep.nci.nih.gov regarding access if you are an authorized user)
Common Data Elements (CDE) Dictionary
Repository of terms to be used when collecting patient information for clinical trials or cancer care
Clinical Data Update System (CDUS)
Mechanism to be used when submitting specified data for clinical trials approved by CTEP (password protected: contact CTEP Help at info@ctep.nci.nih.gov regarding access if you are an authorized user)
Clinical Trials Monitoring Branch - Auditing Information System (CTMS-AIS)
Web-based information system which permits online submission of all data collected during quality assurance audits of NCI-sponsored Cooperative Group clinical trials. The system consists of three modules which link the Cooperative Groups, CTMB, and the Clinical Trials Monitoring Service to Coordinate audit-related activities. (password protected: contact CTEP Help at info@ctep.nci.nih.gov regarding access if you are an authorized user)
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