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THE REVISION OF RP 91 ON CRITERIA FOR ACCEPTABILITY OF RADIOLOGICAL (INCLUDING RADIOTHERAPY) AND NUCLEAR MEDICINE INSTALLATIONS

机译:RP 91对放射学(包括放射治疗)和核医学安装的可接受性标准的修订

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摘要

In 1997 the European Commission published Radiation Protection 91: 'Criteria for acceptability of radiological (including radiotherapy) and nuclear medicine installations'*". This document specified the minimum criteria for acceptability. It has been used to this effect in legislation, codes of practice and by individual professionals. In a single document, it defined a level of performance at which remedial action was required. The document specified a series of parameters which characterised equipment performance and acceptable levels of performance. In its time it proved to be a useful document which was applied in member states to various degrees. Since the publication of Report 91 in 1997, a series of weaknesses emerged over time. Development of new radiological systems and technologies, as well as improvements in traditional technologies, has created circumstances where the acceptability criteria were in need of review. These weaknesses were recognised by the European Commission and a tender for its revision was issued. The criteria were developed by a team drawn from a broad range of backgrounds including hospitals, industry, government bodies, regulators and standardisation organisations. Representatives were mainly from Europe, but individuals from the American Association of Physicists in Medicine and International Atomic Energy Agency were included in the drafting process. This study describes the process employed in developing the revised document and the consultation process involved. One of the major difficulties the revision team encountered was related to an understanding of the actual meaning of the EC Directive. The view taken by the revision team was that Article 8, paragraph 3 places responsibilities on both the holders of radiological equipment and competent authorities. The acceptability criteria have been produced consistent with the European Commission's Medical Exposures Directive, which requires that patient exposures are optimised and justified.
机译:1997年,欧洲委员会发布了《辐射防护91:'放射线(包括放射疗法)和核医学装置的可接受性标准'*”。该文件指定了可接受性的最低标准。在立法,实践准则中已使用此最低标准。在单个文档中,它定义了需要采取补救措施的性能水平,该文档指定了一系列表征设备性能和可接受性能水平的参数,在当时被证明是有用的文档自从1997年第91号报告发布以来,随着时间的推移出现了一系列缺陷,新的放射学系统和技术的发展以及传统技术的改进创造了可接受标准的环境。这些弱点已得到欧盟委员会的认可并发布了修订招标书。该标准是由来自不同背景的团队制定的,这些背景包括医院,行业,政府机构,监管机构和标准化组织。代表主要来自欧洲,但起草过程中包括了美国医学物理学家协会和国际原子能机构的人员。这项研究描述了修订文件的制定过程以及所涉及的咨询过程。修订团队遇到的主要困难之一是与对EC指令实际含义的理解有关。修订小组认为,第8条第3款对放射设备持有人和主管当局均负有责任。可接受标准的制定符合欧洲委员会的《医疗暴露指令》,该指令要求对患者的暴露进行优化和合理化。

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  • 来源
    《Radiation Protection Dosimetry》 |2013年第2期|143-146|共4页
  • 作者单位

    Quality Assurance Reference Centre, North East Strategic Health Authority, Waterfront 4, Goldcrest Way, Newburn Riverside, Newcastle upon Tyne NE15 8NY, UK;

    Trinity Centre for Health Sciences, St James's Hospital, Dublin 8, Ireland;

    Medical Physics Department, Nicosia General Hospital, Nicosia, Cyprus;

    University of Bath, Bath, UK;

    Department of Medical Physics, Royal Surrey County Hospital, Guildford, UK;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
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