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IAC Testifies at FDA Public Hearing on Reduction of Radiation Exposure from Medical Imaging
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As part of its newly announced Initiative to Reduce Unnecessary Radiation Exposure from Medical Imaging, the U.S. Food and Drug Administration (FDA) convened a public meeting on March 30-31 in Maryland. The initiative is a collaborative effort aimed at minimizing the risks associated with exposure to ionizing radiation in certain types of medical imaging procedures, while supporting the benefits these exams can provide. The initiative focuses on the three types of procedures that the FDA states are the greatest contributors to the U.S. population’s total radiation exposure from medical imaging: computed tomography (CT), fluoroscopy and nuclear medicine studies.

Sandra Katanick, CAE, CEO of the Intersocietal Accreditation Commission (IAC), provided testimony during the hearing related to the beneficial role of mandatory imaging accreditation as a tool for use by the FDA, the Centers for Medicare and Medicaid Services (CMS) and the health care professional community in reducing unnecessary radiation exposure from medical imaging. Providing background on the IAC structure and its purpose of providing peer review accreditation through the establishment of quality standards through collaboration with multiple professional medical membership organizations, Ms. Katanick emphasized the role of imaging accreditation on quality measures related to the awareness of and reduction in radiation exposure.

In addition, she discussed the concept of Appropriate Use Criteria (AUC) and the integration of AUC into the accreditation standards to assist providers in evaluating whether the right studies are being performed for the right indications, at appropriate intervals.

Ms. Katanick explained that through imaging accreditation, laboratories are required to document their adherence to mandatory processes that require ongoing oversight and training to help minimize operator error, thus working to ensure safety and quality:

1. Equipment Standards

Mandatory annual physicist survey to evaluate imaging quality, radiation dose utilizing appropriate phantoms, radiation shielding protection survey for CT

Mandatory preventative maintenance of imaging and non-imaging equipment

Comprehensive QC program to assure system performance and image quality

2. Staffing Requirements

All physicians must have modality specific training and experience in image interpretation

All CT technologists must be credentialed and appropriately trained in modality specific imaging

All staff must maintain modality specific CME

Physicist's participation is required for protocol development, system performance and dose assessment for patients and personnel


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volume 3, issue 1
spring 2010

headlines from the IAC

  • IAC Receives Designation by CMS as Accrediting Organization for MIPPA
  • IAC Testifies at FDA Public Hearing on Reduction of Radiation Exposure from Medical Imaging
  • IAC Participates in Advanced Imaging Accreditation Meeting with CMS
  • IAC to Incorporate Measurement of Appropriate Use Criteria (AUC)
  • Maintaining Compliance
  • Changes in 2010
  • Board News: Changes in IAC Leadership
  • Celebrating IAC: 20 Years of Laboratory Accreditation
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