Clinical Trials Management Systems (CTMS) Workspace
The Clinical Trials Management Systems (CTMS) Workspace is developing a comprehensive set of modular, interoperable and standards-based tools designed to meet diverse clinical trials management needs and respond to four informatics-focused recommendations made by NCI's Clinical Trials Working Group (CTWG). For more information on the CTWG's four informatics-focused recommendations, click here. Looking for information on how caBIG™ helps facilitate clinical data management and data sharing Check out the Clinical Trials Compatibility Framework New to the Clinical Trials Management Systems (CTMS) Workspace? Check out the CTMS Newcomer Information section. Registration for the March 18-20, 2008 Joint CTMS & Imaging Face-to-Face meeting is now open. To register online, please go to Joint CTMS & Imaging Face-to-Face registration page. Looking for a review of recent caBIG™ activities? caBIG™ Links: The monthly newsletter provides brief articles on ways in which institutions are implementing caBIG™ products, as well as recent developments in the caBIG™ initiative. CTMS MaterialsSchedule (for teleconferences) Workspace Teleconference Meeting Notes Face-to-Face Meeting Materials (2004 to present) CTMS Participating Organizations Templates & Forms (internal working templates and forms for participants and adopters.) CTMS home on GForge (GForge is a separate collaborative working area utilized by many caBIG™ workspaces to collect and organize additional materials) CTMS Special Interest Groups (SIGs)The Planning / Monitoring SIG aims to facilitate the planning and initiation of clinical trials and the monitoring of trials once they begin. Activities include: - Investigator and Site Credential Repository - Study Initiation Tool - Federal Investigator Registry of Biomedical Informatics Research Data (FIREBIRD) - Protocol Lifecycle Tracking - NCI Division of Cancer Prevention's Enterprise System Knowledgebase (DESK)
The Study Conduct SIG addresses issues related to the conduct of clinical trials. Activities include: - Standardized Case Report Forms - Cancer Central Clinical Database (C3D) - Participant Registry - Subject Prescreening - Vendor Systems
The goal of the Reporting / Sharing SIG is to facilitate the reporting and sharing of clinical trial data with existing and new destinations. Activities include: - Clinical Trials Object Model - Janus (FDA Repository)
This SIG aims to achieve interoperability by increasing the ability of systems to access and use the data and functionality of other systems and facilitating the integration of new sources and destinations of data. Activities include: - Structured Protocol Representation (BRIDG) - Clinical Trials Interoperability Project
Archived SIGs and Work Groups: - Adverse Event Reporting and Collection - SOPs - System Interoperability & Harmonization | CTMS Participant Shortcuts
CTMS Product ShortcutsTools
To see a list of all caBIG™ tools, visit the Tools page InfrastructurePolicies, Guidelines and WhitepapersTo see a list of all caBIG™ policies and guidelines, visit the Policies, Guidelines & Whitepapers section. |