What laws and regulations apply to the manufacture and sale of pharmaceuticals and medical products in China?

The laws and regulations governing the manufacture and sale of pharmaceuticals and medical products in China are determined by the State Council and other government bodies. According to the Drug Administration Law and the Good Manufacturing Practice (GMP) regulations, all pharmaceutical products must be manufactured and sold in accordance with a series of quality standards and safety regulations. In order to ensure the safety and efficacy of drugs, as well as to provide reliable, safe, and effective drugs to the population, the State Council and other government bodies in China have implemented a series of laws and regulations related to pharmaceuticals and medical products. Before drugs can be sold, they must be registered with the State Food and Drug Administration (SFDA). In addition, manufacturers must obtain a GMP certification from the SFDA, to ensure that the manufacturing process is in compliance with the requirements. Finally, pharmaceuticals and medical products must also adhere to regulations and standards regarding the packaging, labeling, and advertisement of the products. These regulations ensure that consumers are provided with accurate and clear information about the products. In addition, all promotional materials must be approved by the State Administration for Industry and Commerce (SAIC). Overall, the Chinese government has implemented a comprehensive set of laws and regulations to ensure the quality and safety of pharmaceuticals and medical products, to provide reliable and effective drugs to the population, and to protect consumers from false or misleading information.

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What laws and regulations apply to the manufacture and sale of pharmaceuticals and medical products in China?

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