Activities | - Briefly review the role and expectations of the QMP as MR safety expert consultant with emphasis on assessment and formulation of a plan of action for patient scanning in the presence of devices or medical implants.
- Review relevant physics for understanding MR safety concerns of medical devices and implants.
- Review published literature & standards for medical device and implant evaluation in MR environment.
- Outline methods and promote best practices for evaluating medical devices for use in patients as well as reporting of results by QMP.
- Outline methods and promote best practices for QMP evaluation of risk in patients with implanted medical devices (active and passive) as well as reporting and communication considerations with staff
and/or clinicians. - Outline general considerations and approaches to modifying MR acquisitions to accommodate conditions for MR safety versus imaging quality or indication.
- Identify potential pitfalls and areas requiring research or better standardization
- Provide recommended standard operating procedures and checklists for specific device categories (with examples).
- Publish a Task Group report.
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By-Laws: | Not Referenced.Rules: Not Referenced. |
Standing? | This is not a standing committee. |
Approved Date(s): | 12/19/2019 - 12/31/2025
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Reviewable Draft Deadline: | |
Committee Keywords: |
No Keywords Entered
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Chair
R. Jason Stafford Task Group Chair
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2025 Roster
(dates shown below are start and end dates of position.)

= complete and up-to-date

= up-to-date but expires soon

= incomplete or out of date conflict of interest statement.
VOTING Appointments | There are 7 voting members. |