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ublic health;Qualifications;Qualitative;Quality management;Quantitative;Risk;Risk analysis;Safety;Safety measures;Safety tests;Specification (approval);Surveillance (approval);Use【摘要】: This International Standard specifies a process for a manufacturer to identify the hazards associated with medical devices, including in vitro diagnostic (IVD) medical devices, to estimate and evaluate the associated risks, to control these risks, and to monitor the effectiveness of the controls.The requirements of this International Standard are applicable to all stages of the life-cycle of a medical device.This International Standard does not apply to clinical decision making.This International Standard does not specify acceptable risk levels.This International Standard does not require that the manufacturer have a quality management system inplace. However, risk management can be an integral part of a quality management system.【中国标准分类号】: C37【国际标准分类号】: 11_040_01【页数】: 96P.;A4【正文语种】: 英语 | 欢迎光临 世界资料网论坛 (http://bbs.infoeach.com/) | Powered by Discuz! X2.5 |