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          CFDA Announcement on Releasing GoodManufacturing Practice for Medical Devices

          Keyword: CFDA   Announcement   on   Releasing  
          Inputtime:January 14,2018


          Original link: http://www.sda.gov.cn/WS01/CL0087/111642.html

          China Food and Drug Administration
          Announcement

          [2014] No. 64

          Announcement on Releasing Good Manufacturing Practice for Medical Devices

          In order to enhance the supervision and administration of, and standardize thequality management of, the medical devices manufacturing, and in accordance with the Regulations for the Supervision and Administration of Medical Devices ( StateCouncil Order No. 650) and the Provisionfor Supervision of Medical DevicesManufacturing (CFDA Order No. 7), China Food and Drug  Administration(“CFDA”) organized the revision of the GoodManufacturing Practice for Medical Devices, and which is hereby released.

            It is hereby notified!

            Annex: Good Manufacturing Practice for Medical Devices

                                          China Food and Drug Administration
                                          December 29, 2014

            

          Annex

          Good Manufacturing Practice for Medical Devices

          Chapter I General Provisions

          Article 1    
          With a view to ensuring the safety and effectiveness of medical devices and standardizingthe management on quality of medical devices manufacturing, the  
          GoodManufacturing Practice for Medical Devices (“GMP”) is hereby formulated inaccordance with Regulations for the Supervision and Administration of Medical Devices (State Council Order No.650) and the Provision for Supervision of Medical Devices Manufacturing (CFDA Order No. 7).

          Article 2    
          Medical device manufacturers (hereinafter referred to as “manufacturers”) shall comply with the requirements set out in the GMP when designing and developing,manufacturing and selling medical devices, as well as providing after-sales services. 

          Article 3    
          Manufacturers shall establish and improve the quality management system adapted to the medical devices manufactured in combination with product features according to the requirements in the GMP and ensure its effective operation.

          Article 4    
          Manufacturers shall conduct risk management through the whole process of design and development,manufacture, sales and after-sales service and take the measures adapted toproduct risks.

          For full text please click on the link:http://www.sda.gov.cn/WS01/CL0087/111642.html

           

           

           

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