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1998年发布了《乳房X线摄影质量标准法案》(MQSA)最终规定。美国放射学会。

1998 MQSA (Mammography Quality Standards Act) final rule released. American College of Radiology.

出版信息

Radiol Manage. 1998 Jul-Aug;20(4):51-5.

Abstract

In October 1997, the Food and Drug Administration (FDA) released the final regulations for implementing the Mammography Quality Standards Act (MQSA). Briefly, the final rule establishes experience requirements for medical physicists and radiologic technologists and clarifies equipment standards. The Interim Rules, issued in late 1993 and amended in 1994, now apply. Final regulations become effective April 1999, with certain equipment regulations becoming effective in October 2002. Changes in experience and continuing education requirements for medical physicists and radiologic technologists parallel requirements in the interim rule. The FDA shifted the majority of quality assurance requirements for equipment to the quality assurance section of the regulations, and will treat them as performance standards. Under the final rule, each facility is required to have a system to ensure that mammogram exam results are communicated to patients in a timely manner. Under the interim regulations, mammography facility personnel must continue to participate in medical education programs in mammography to acquire five CME/CEU per year.

摘要

1997年10月,美国食品药品监督管理局(FDA)发布了实施《乳房X线摄影质量标准法案》(MQSA)的最终规定。简而言之,最终规则确立了医学物理学家和放射技师的经验要求,并明确了设备标准。1993年末发布并于1994年修订的暂行规则现仍适用。最终规定于1999年4月生效,某些设备规定于2002年10月生效。医学物理学家和放射技师在经验和继续教育要求方面的变化与暂行规则中的要求一致。FDA将设备的大部分质量保证要求转移到了法规的质量保证部分,并将其作为性能标准对待。根据最终规则,每个机构都必须有一个系统,以确保乳房X线摄影检查结果能及时传达给患者。根据暂行规定,乳房X线摄影机构的人员必须继续参加乳房X线摄影方面的医学教育项目,每年获得5个继续医学教育学分/继续教育单元。

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