The Cancer Center Participant Registry (C3PR)

The Cancer Center Participant Registry (C3PR) is a web-based application used for end-to-end registration of patients to clinical trials. This includes capturing the consent signed date, eligibility criteria, stratification, randomization, and screening. C3PR also enables multi-site clinical trials where registration information is entered locally at affiliate sites and the registration is completed by call-out to the coordinating site. It is used to improve clinical trials activation and execution by providing an efficient Web-based clinical trials information management system available for use by multiple cancer research centers, and can support large-scale, geographically dispersed studies.
FEATURES:
• Manages subject registrations to clinical trials (study open, participant eligible, consent received)
• Stratifies subjects, randomizes to trial arms, registers subjects to companion protocols
• Streamlines registration workflow by provider role-based views to registration data
• Notifies users through email and dashboard of registration events, including accrual thresholds
• Tracks participants across sites and handles single-site and multi-site trials
• Manages study personnel who have access to registry
• Reports data to facilitate generation of NCI Cancer Center Summary 3 and 4 reports
• Facilitates compliance with Federal regulations including 21 CFR Part 11, HIPAA, and Section 508
• Integrates with other clinical systems

Visit : http://www.healthcit.com/front/caBIG/node/69