中国医疗器械杂志2024,Vol.48Issue(2) :212-216.DOI:10.12455/j.issn.1671-7104.230405

医用电子直线加速器生产环节风险分析及现场体系核查要点

Production Risk Analysis and Key Points for Field Inspection of Medical Electron Linear Accelerator

杨义强
中国医疗器械杂志2024,Vol.48Issue(2) :212-216.DOI:10.12455/j.issn.1671-7104.230405

医用电子直线加速器生产环节风险分析及现场体系核查要点

Production Risk Analysis and Key Points for Field Inspection of Medical Electron Linear Accelerator

杨义强1
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作者信息

  • 1. 上海市医疗器械化妆品审评核查中心,上海市,200020
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摘要

医用电子直线加速器具有系统结构复杂、核心部件多、控制精度要求高等特点,对产品质量控制和监管都提出了较高的要求.该研究通过对医用电子直线加速器技术特点及生产环节风险分析,结合医疗器械生产质量管理规范要求,提出了此类产品现场体系检查要点,对企业的质量管理人员和监管部门的检查员具有一定参考意义.

Abstract

The medical electron linear accelerator(LINAC)has the characteristics of complex system structure,many core components and high precision control requirements,which puts forward higher requirements for product quality control and regulation.This study puts forward the main points of field inspection through the analysis of the technical characteristics and production risk of LINAC,combined with the requirements of the good manufacturing practice of medical devices.It has certain reference significance for quality management personnel and field inspectors.

关键词

医用电子直线加速器/生产风险/现场体系核查/生产质量管理规范

Key words

medical electron linear accelerator(LINAC)/production risk/field inspection/good manufacturing practice

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出版年

2024
中国医疗器械杂志
上海市医疗器械检测所

中国医疗器械杂志

CSTPCD
影响因子:0.503
ISSN:1671-7104
参考文献量16
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