Because China is a society ruled by law, all walks of life should abide by the law, and so should the pharmaceutical industry. Learning drug laws and regulations is not to engage in drug management, but to know and abide by the law.

According to the definition of drugs in Article 2 of the Drug Administration Law of People's Republic of China (PRC), drugs mentioned in this Law refer to substances used to prevent, treat and diagnose human diseases, purposefully regulate human physiological functions, and specify indications or functional indications, usage and dosage, including traditional Chinese medicines, chemicals and biological products.

20 13, 1 the national development and reform commission issued a notice, and decided to adjust the maximum retail price limit of respiratory drugs, antipyretic and analgesic drugs, specialty special drugs and other drugs from February 20 13. * * * involving 20 kinds of drugs, more than 400 varieties, more than 700 representative dosage forms, with an average price reduction of 65438.

The new drug administration law has been revised and passed, and will be implemented on 20 19 12 1. 202 1 February, the Supreme People's Court and the Supreme People's Procuratorate on the implementation

On the user side, it is aimed at preventing, treating and diagnosing human diseases. Purposefully regulating people's physiological functions, with specified indications, usage and dosage requirements; From the way of use: in addition to the appearance of patients can not identify their internal quality, many drugs need to be used under the guidance of doctors, rather than by the choice of patients.

At the same time, the use method, quantity, time and other factors largely determine the use effect. Misuse can not only "cure", but also "cause disease" and even endanger life safety. Therefore, medicine is a special commodity.