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SFDA further intensifies and standardizes the registration of medical devices
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To further intensify and standardize the registration of medical devices, solidify the achievement of special rectification of medical devices, and guarantee the safety and effectiveness of medical devices, in accordance with Regulations for the Supervision and Administration of Medical Devices and Provisions for Medical Device Registration and according to the actual conditions of the registration of medical devices, the State Food and Drug Administration (SFDA) issued the Interim Requirements for Further Intensifying and Standardizing the Registration of Medical Devices on July 23,2008. The Interim Requirements took effect on the date of issuance.
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