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(huì)的注冊會(huì)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(huì)，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(jià)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.