2, in addition to the existing 17 Chinese herbal medicine professional market, all localities shall not open a new Chinese herbal medicine professional market. The local people's government of the specialized market of Chinese herbal medicines shall, in accordance with the principle of "who manages, who manages", assume the management responsibility and clarify the market subject and its responsibilities.
3. It is strictly prohibited to sell fake and inferior Chinese herbal medicines, to operate Chinese herbal pieces, proprietary Chinese medicines and other medicines in any name or manner without approval, to sell 27 kinds of toxic medicinal materials specified by the state, and to illegally sell 42 kinds of endangered medicinal materials specified by the state.
4. It is strictly prohibited to engage in activities such as sub-packaging and label changing of decoction pieces. It is strictly forbidden to purchase Chinese herbal pieces from the Chinese herbal medicine market or other units or individuals that do not have the qualifications for the production and operation of Chinese herbal pieces to ensure the safety of Chinese herbal pieces.
5. It is strictly forbidden for Chinese patent medicines and related drugs that are prohibited from entering the market by the state to enter the Chinese herbal medicine market, to prohibit the manufacture and sale of counterfeit and shoddy drugs, and to maintain the market operation order.
6. 17 The specialized markets of Chinese herbal medicines are distributed in Baoding, Harbin, Heilongjiang, Bozhou, Anhui, Yichun, Jiangxi, Heze, Shandong, Xuchang, Henan, Huanggang, Hunan, Changsha, Shaoyang, Guangzhou, Jieyang, Yulin, Guangxi, Yuzhong, Chongqing, Chengdu, Sichuan, Kunming, xi, Shaanxi.
Legal basis:
Article 14 of the Drug Administration Law shall meet the requirements for the rational distribution of drug wholesale enterprises in provinces, autonomous regions and municipalities directly under the Central Government, and meet the following standards: (1) There are rules and regulations to ensure the quality of drugs handled; (2) The enterprise and its legal representative or the person in charge of the enterprise and the person in charge of quality management have no circumstances as stipulated in Articles 75 and 82 of the Drug Administration Law; (3) Having a certain number of licensed pharmacists suitable for the business scale. The person in charge of quality management has a college degree or above and must be a licensed pharmacist; (4) Having normal-temperature warehouses, refrigerated warehouses and frozen warehouses that meet the quality requirements for drug storage and are suitable for its business variety and scale. The warehouse has special shelves suitable for drug storage and devices and equipment of modern logistics system for drug storage, transportation, sorting, shelving and delivery; (5) Having an independent computer management information system, which can cover the whole process of drug procurement, storage, sales, management and quality control; Information that can comprehensively record the enterprise management and the implementation of the "Good Manufacturing Practices"; It meets the requirements of "Quality Management Standards for Drug Trading" on all aspects of drug trading, and has the conditions to accept the supervision of local food and drug supervision and management departments; (6) It meets the requirements of drug business premises and auxiliary facilities, management of office buildings and warehouses, quality and safety guarantee of drugs in warehouses, storage and maintenance of drugs in warehouses. If the state has other provisions on dealing in narcotic drugs, psychotropic drugs, toxic drugs for medical use and biological products for prevention, those provisions shall prevail.