Page History
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- Information for CTRP Application Users
- CTRP User Meetings - information, including meeting schedules and notes
- COPPA Core Services - information about, and instructions for accessing and using CTRP core services
- Information About the CTRP Project
- Application Release Plans and Schedules - information, including release notes for past and current releases; plans for future releases; and recurring meeting schedules
- CTRP Environments and Tiers - outlines the policies and procedures the CTRP team follows internally when deploying software to various tiers
- CTRP Project Team - lists project team members and their roles
- Overview of CTRP Applications - introductory information about applications, including those available for use by individuals registered in CTRP, and those for use by internal NCI/CTRP application specialists
- Information for CTRP Application Developers - information for developers and consumers of COPPA core services
- CTRP Dev Team Meeting Notes
- Technical Notes - provides design and development information for developers and architects
About CTRP
NCI's Clinical Trials Reporting Program (CTRP) fulfills a recommendation made by the NCI Clinical Trials Working Group (CTWG) to the National Cancer Advisory Board. The purpose of the program is to establish a comprehensive database containing regularly updated information on all NCI-funded clinical trials. Grantees enter specific information about each clinical trial into the database. NCI internally transfers to CTRP information on CTEP, CCR and DCP trials, eliminating the need for awardees to enter information on these trials. NCI uses this information to coordinate research efforts to optimize our nation's investment in cancer research. NCI initiated a phased launch of CTRP, which started January 2009, with a focus on registering interventional trials only. The registration of observational, ancillary and correlative studies will begin at a later date.
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