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SFDA specifies relevant requirements on application for alternation of the registration certificate of medical devices
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To further intensify the management of the registration of medical devices, standardize the order of the registration of medical devices, simplify administrative procedures and make administrative licensing application convenient for applicants, the State Food and Drug Administration (SFDA) recently issued Notice on Relevant Requirements on Application for Alternation of the Registration Certificate of Medical Devices in accordance with Provisions for Medical Device Registration and Provisions for the Instructions, Labels and Package of Medical Devices, to specify and explain the requirements on application for alternation of the registration certificate of medical devices.
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