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Study Conduct SIG
The Study Conduct SIG facilitates the conduct of clinical trials. This SIG is also responsible for the CTWG informatics initiative to achieve concurrence on standard Case Report Forms. The Study Conduct SIG is part of the Clinical Trials Management Systems (CTMS) Workspace. The Study Conduct SIG contains work groups focused on specific projects and tools: - Standardized Case Report Forms - Cancer Central Clinical Database (C3D) - Participant Registry - Subject Prescreening - Vendor Systems Who should get involved?The Study Conduct 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 Study Conducts 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: Tom Ehlman (ehlmantn@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.) | Study Conduct SIG Participant ShortcutsStudy Conduct Task Force Participant ShortcutsRelated Products
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