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        注冊檢驗 Production Registration

        翔康技術注冊員工均為相關產品標準技術委員會的注冊會員,每年定期參加CFDA組織的產品技術要求、標準研討會,熟悉醫用電氣設備安全通用要求、醫療器械生物學評價要求等各種國家標準及行業標準和檢定規程。致力于醫療器械和診斷試劑類產品的國內外標準以及法規的研究,并且與各省局醫療器械檢測中心保持良好合作關系,為您提供醫療器械及診斷試劑類產品全方位的注冊解決方案!

        Xiangkang
        Biotech registrars are all registered members of relevant product standards
        technical committee. They regularly participate in the product technical
        requirements and standards seminar organized by NMPA every year. They are
        familiar with various national standards and industry standards and
        verification regulations, such as general safety requirements for medical
        electrical equipment and biological evaluation requirements for medical
        devices. Committed to the domestic and foreign standards and regulations of
        medical devices and diagnostic reagent products, and maintain a good
        relationship with provincial medical device testing center, to provide you with
        a full range of medical devices and diagnostic reagent products registration
        solutions.

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