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What will happen if the labels of backup drugs are not consistent?

The consequence is that you will be subject to administrative penalties from the Food and Drug Administration for drug labeling that does not comply with regulations. According to the public information inquiry on the relevant drug labeling management regulations, a single labeling error will result in administrative penalties, and an error resulting in disability or death will result in the revocation of the medical drug qualification certificate and prosecution. According to the definition of drugs in Article 2 of the Drug Administration Law of the People's Republic of China and the People's Republic of China, drugs as mentioned in this Law refer to drugs used to prevent, treat, and diagnose human diseases, purposefully regulate human physiological functions, and provide for adaptation. Substances with symptoms or functions, usage and dosage, including traditional Chinese medicine, chemical drugs and biological products.