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          1. 注冊檢驗 Production Registration

            翔康技術(shù)注冊員工均為相關(guān)產(chǎn)品標(biāo)準(zhǔn)技術(shù)委員會的注冊會員,每年定期參加CFDA組織的產(chǎn)品技術(shù)要求、標(biāo)準(zhǔn)研討會,熟悉醫(yī)用電氣設(shè)備安全通用要求、醫(yī)療器械生物學(xué)評價要求等各種國家標(biāo)準(zhǔn)及行業(yè)標(biāo)準(zhǔn)和檢定規(guī)程。致力于醫(yī)療器械和診斷試劑類產(chǎn)品的國內(nèi)外標(biāo)準(zhǔn)以及法規(guī)的研究,并且與各省局醫(yī)療器械檢測中心保持良好合作關(guān)系,為您提供醫(yī)療器械及診斷試劑類產(chǎn)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.