FDA Perspective on Radiation Dose Monitoring

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Nothing to Disclose. . 21 USC 360ii. FDA has authority to: Plan, conduct, coordinate, and support research, development, training and operational activities to minimize the emissions of and the exposure of people to, unnecessary electronic product radiation. Goals. National dose registryNatio

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FDA Perspective on Radiation Dose Monitoring

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1. FDA Perspective on Radiation Dose Monitoring ACR Dose Monitoring Forum Donald L. Miller, M.D. FACR Acting Chief, Diagnostic Devices Branch Division of Mammography Quality and Radiation Programs Center for Devices and Radiological Health Food and Drug Administration

2. Nothing to Disclose

3. 21 USC 360ii FDA has authority to: Plan, conduct, coordinate, and support research, development, training and operational activities to minimize the emissions of and the exposure of people to, unnecessary electronic product radiation

4. Goals National dose registry National reference levels

5. FDA Dose Reduction Initiative The healthcare professional community, in collaboration with FDA, should continue efforts to develop DRLs for CT, fluoroscopy, and nuclear medicine procedures locally and also through a national radiation dose registry. Requirements for CT and fluoroscopic device capability to record radiation dose information for use in patient medical records or a radiation dose registry. Provide patients with tools to track their personal medical imaging history.

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