国产日韩欧美综合一区_ Medical device registration company, medical device third party registration service, medical device business license processing center, Hangzhou certification standard guest Enterprise Management Co., Ltd. official website

Registration Service of Medical Devices: CRC services Medical Device Business License Medical Device Registration Contract Research Organization ISO 13485 Quality System Certification GMP CE Certification Service FDA Registration (Filing) Software Integrity Verification Service Production process validation service ISO 15378 Medical Package System Certification ISO 13485 Internal Auditors Training Regulatory Services For Medical Devices
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Medical Software Development: Software of Good Supply Practice(GSP) Production System Development Customized software development

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ISO13485 (YY/T0287) 內審員培訓服務(wù)簡(jiǎn)介 ISO13485：2016《醫療器械質(zhì)量管理體系用于法規的要求》標準，是應用于醫療器械專(zhuān)用的獨立標準，強調滿(mǎn)足醫療器械法規要求，隨著(zhù)歷史的發(fā)展，ISO組織將此標準進(jìn)行了修訂，升級為ISO13485：2016于2016年7月15日發(fā)布。國家食品藥品監督管理局已按等同采用的原則轉化為行業(yè)標準YY/T0287-2016。在歐洲歐洲市場(chǎng)上醫療器械生產(chǎn)廠(chǎng)商被強制要求通過(guò)認證機構的CE認證。 Time:2018-6-29 11:39:45 View:2779