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Reporting / Sharing SIG
The aim of the Reporting / Sharing SIG is to facilitate the reporting and sharing of clinical trial data to existing/new destinations. This SIG is also responsible for addressing the CTWG informatics initiative related to the establishment of a comprehensive database containing regularly-updated information on all NCI-funded clinical trials. The Reporting / Sharing SIG is part of the Clinical Trials Management System (CTMS) Workspace. The Reporting / Sharing SIG consists of several work groups focused on specific projects: - Clinical Trials Object Model - Janus (FDA Repository) - Adverse Event Reporting and Collection
Who should get involved?The Reporting / Sharing SIG encourages anyone who is interested and/or involved in the conduct, administration, and regulation of clinical trials. These include, clinical trialists, clinical investigators, research nurses, informaticists, clinical trial sponsors, IRB and FDA representatives. These and others are key stakeholders whose input, review and feedback is imperative to the successful development and deployment of applications to support clinical trials and enable improved exchange of clinical trial information. Individuals interested in participating are invited to join the Reporting / Sharing SIG Listserv. The Listserv serves as the primary means of communication for the SIG. Meeting announcements are posted to the Listserv prior to the meeting.
Contact InformationSIG Lead: John Speakman (speakmaj@mail.nih.gov) Ed Helton (heltone2@mail.nih.gov) SIG Facilitator: Michele Elhman(Ehlmanmr@mail.nih.gov ) (Note: The SIGs in the CTMS Workspace were re-organized in May 2007. Some of the current Work Groups were formerly known as SIGs; however, the terminology used on documents developed prior to May 2007 will not be changed to reflect the current organizational structure of the CTMS Workspace.) | Reporting / Sharing SIG Participant ShortcutsReporting / Sharing Task Force Participant ShortcutsRelated Products
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