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      注冊檢驗 Production Registration


      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