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SFDA solicits opinions on the Interim Requirements for Further Intensifying and Standardizing the Registration of Medical Devices (draft for comments)
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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, The State Food and Drug Administration (SFDA) drafted the Interim Requirements for Further Intensifying and Standardizing the Registration of Medical Devices (draft for comments) in accordance with Regulations for the Supervision and Administration of Medical Devices and Provisions for Medical Device Registration and in combination of the actual conditions of the registration of medical devices. SFDA is now soliciting opinions and suggestions on the Interim Requirements.
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