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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