- To review the literature and summarize the historical development of HIFU therapy, clinical findings to date, and current trends in research.
- To review relevant clinical products and describe the components in detail with an assessment of capabilities and current technology limitations.
- To recommend standards for quality assurance and quality management, including commissioning, periodic QA, patient-specific QA, and periodic QM.
- To determine criteria for designing and establishing an FUS facility including equipment, personnel resources, protocols, and credentialing.
- To recommend documentation standards for prescribing, reporting, and recording MRgFUS treatment data.
|Bylaws:||Not Referenced.Rules: Not Referenced.
|Approved Date(s)||Start: 9/21/2009
Task Group Chair
Task Group Co-Chair
2016 RosterView 2015 Roster
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