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SFDA implements catalogue management to the production of some export drugs and medical devices
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In order to strengthen the supervision to export drugs and medical devices, and ensure product quality and safety, the State Food and Drug Administration (SFDA) decided to implement catalogue management to the production of some export drugs and medical devices in accordance with the Drug Administration Law of the People's Republic of China, and the Special Regulations of the State Council on Intensifying Safety Control of Food and Other Products. SFDA will formulate, promulgate, and regulate the Product Catalogue for Export Drugs and Medical Devices Supervision on the basis of work requirements of supervision and administration. SFDA recently issued an announcement and publicized the first Product Catalogue for Export Drugs and Medical Devices Supervision, which includes 9 categories of drug raw materials and preparations and two categories of medical devices, and specified relevant issues.
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