电议
Quality System Regulation, Medical Devices Quality System Regulation, Medical Devices FDA 21 CFR Part 820
Quality System Regulation, Medical Devices Quality System Regulation, Medical Devices FDA 21 CFR Part 820
检测项目
- Quality System Regulation, Medical DevicesQuality System Regulation, Medical Devices FDA 21 CFR Part 820-
支持报告类型： 电子报告、纸质报告
支持报告语言： 中文报告、英文报告、中英文报告
报告盖章资质： CMA；CNAS
服务周期： 3-10个工作日（特殊样品除外）
服务地区： 全国
检测用途： 电商平台入驻；商超卖场入驻；产品质量改进；产品认证；出口通关检验等
取样方式： 快递邮寄或上门取样
样品要求： 样品数量及规格等视检测项而定
服务详情
检测标准
检测项目 Quality System Regulation, Medical Devices
检测标准号 FDA 21 CFR
检测方法名 Quality System Regulation, Medical Devices FDA 21 CFR Part 820
限制说明
服务简介
服务范围：GB、GB/T、FZ/T品控检测、各类电商平台、商超卖场入驻质检。
服务流程
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报告样例
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百检介绍
相关标准
《EN ISO 13485》Medical Devices Quality management systems –Requirements for Regulatory Purposes EN ISO 13485
《IEC62366-1:2015》Medical devices-Part 1:Application of usability engineering to medical devices
《FDA 21 CFR820》MEDICAL DEVICESPART 820QUALITY SYSTEM REGULATION FDA 21 CFR820
《ISO 13485:2016》Medical Devices Quality management systems –Requirements for Regulatory Purposes ISO 13485:2016
《FDA 21 CFR Part 820》Quality System Regulation, Medical Devices FDA 21 CFR Part 820
《DIN EN ISO 13485》Medical Devices Quality management systems –Requirements for Regulatory Purposes DIN EN ISO 13485
《FDA 21CFR820》Quality System (QS) Regulation/Medical Device Good Manufacturing Practices FDA 21CFR820
《ISO 13485》Medical Devices Quality management systems –Requirements for Regulatory Purposes ISO 13485
《FDA QSR 820》FDA 21 CFR Part 820, Quality System (QS) Regulation/Medical Device Good Manufacturing Practices FDA QSR 820
《ISO 13485:2016》Medical Devices-Quality management systems –Requirements for regulatory puroses ISO 13485:2016
《IEC62366-1:2015》Medical devices-Part 1:Application of usability engineering to medical devices
《FDA 21 CFR820》MEDICAL DEVICESPART 820QUALITY SYSTEM REGULATION FDA 21 CFR820
《ISO 13485:2016》Medical Devices Quality management systems –Requirements for Regulatory Purposes ISO 13485:2016
《FDA 21 CFR Part 820》Quality System Regulation, Medical Devices FDA 21 CFR Part 820
《DIN EN ISO 13485》Medical Devices Quality management systems –Requirements for Regulatory Purposes DIN EN ISO 13485
《FDA 21CFR820》Quality System (QS) Regulation/Medical Device Good Manufacturing Practices FDA 21CFR820
《ISO 13485》Medical Devices Quality management systems –Requirements for Regulatory Purposes ISO 13485
《FDA QSR 820》FDA 21 CFR Part 820, Quality System (QS) Regulation/Medical Device Good Manufacturing Practices FDA QSR 820
《ISO 13485:2016》Medical Devices-Quality management systems –Requirements for regulatory puroses ISO 13485:2016
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