The State Food and Drug Administration implements a catalogue management on the production of some exported drugs and medical devices to strengthen the supervision of exported drugs and medical devices to ensure product quality and safety.
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The State Food and Drug Administration reported on October 24th that in order to strengthen the supervision over the export of medicines and medical devices and ensure the quality and safety of products, it is based on the "Drug Administration Law" and the "Special Provisions of the State Council on Strengthening the Supervision and Administration of the Safety of Food Products," National Foods. The drug administration bureau decided to implement catalogue management for the production of certain types of exported drugs and medical devices, and formulates, publishes, and adjusts the “Catalogue of Regulated Products of Exported Pharmaceuticals and Medical Devices†according to the needs of supervision and management work.
Recently, the State Food and Drug Administration issued a notice and announced the list of the 9 categories of pharmaceutical raw materials, pharmaceutical preparations, and 2 types of medical devices listed in the "Catalogue of Listed Products for the Control of Exported Pharmaceuticals and Medical Devices" and clarified relevant issues.
The State Food and Drug Administration implements the catalogue management of the production of some exported drugs and medical devices