The medical institutions referred to in the preceding paragraph, including hospitals, maternal and child health centers, health centers, sanatoriums, outpatient clinics (including individual), clinics (including individual), health centers (rooms), emergency centers (stations), hospitals for the prevention and control of disease (station), nursing homes (station), community health service centers (station), and other diagnostic and treatment institutions engaged in disease prevention, diagnosis, treatment, health care activities, and family planning technical services. Article 3 Article 3 The food and drug administration department of the provincial people's government is responsible for the supervision and management of the province's medical institutions drugs and medical devices. Municipal, county and district people's government food and drug supervision and management department is responsible for the supervision and management of medical institutions within the administrative area of drugs and medical devices.
The relevant administrative departments of the people's governments at or above the county level are responsible for the supervision and management of drugs and medical devices in medical institutions within their respective areas of responsibility. Article IV of the medical institutions shall be approved in accordance with the law of the diagnosis and treatment subjects, family planning technical services within the scope of the use of drugs, with a licensed physician, physician assistant or obtain a certificate of registration of rural doctor practice of rural doctors to dispense medicines. Article 5 medical institutions may, in accordance with relevant state regulations, in accordance with the approved diagnostic and treatment subjects and the use of drugs within the scope of the pharmacy or medicine cabinet.
Medical institutions set up a pharmacy or medicine cabinet, should be consistent with the provincial people's government food and drug supervision and management departments to develop management specifications. Article VI individual clinics, clinics and other medical institutions, shall not be equipped with commonly used drugs and first aid drugs other than drugs. The scope and varieties of commonly used medicines and first-aid medicines shall be formulated and announced by the health administrative department of the provincial people's government in conjunction with the food and drug supervision and management department of the provincial people's government.
The scope of drugs used in family planning technical service institutions shall be consistent with the approved scope of services, services, surgical procedures, and shall not use drugs other than the basic drug list of family planning technical service institutions, except for those who have obtained a medical practice license. The basic medication list of family planning technical service institutions shall be formulated and announced by the food and drug administration department of the provincial people's government in conjunction with the family planning administrative department of the provincial people's government. Article 7 The scope and varieties of drugs used by medical institutions as stipulated in Article 6 of these Measures shall not be changed without authorization. Need to change, should be reported to the local food and drug supervision and management departments, health administrative departments or family planning administrative departments for approval. Article VIII of the medical institutions shall have a "drug production license" or "drug business license" of the drug production and business enterprises to purchase drugs, except for the implementation of the approval number management of Chinese herbal medicines. Village health office, individual clinics can also be entrusted to the township health center on behalf of the procurement of drugs or by the local drug distribution center for distribution.
The township health center to purchase drugs on behalf of the village health center, individual clinics should hold a letter of entrustment issued by the local food and drug supervision and management departments to accept the supervision and inspection. Article IX of the medical institutions to purchase drugs, should establish a purchase inspection and acceptance system, inspection of drug certificates of conformity and other packaging identification; does not meet the prescribed requirements, shall not be purchased. Article 10 medical institutions shall, in accordance with the provisions of laws and regulations, the establishment of true and complete records of drug purchases. Drug purchase records shall be kept for not less than 3 years; drug expiration date of more than 3 years, save to the expiration of 1 year after the expiration date of the drug. Article XI of the medical institutions shall dispense medicines by prescription, shall not be mailed, forged prescriptions, counter open shelf self-selection and charity clinics, charity sales, consulting, trial, trade fairs, and other ways of operating or disguised as operating medicines. Article XII of the medical institutions shall develop and implement the drug storage system, in accordance with the provisions of the quality and safety of drugs classified storage, to take refrigeration, anti-freezing, moisture, light, ventilation, fire prevention, pest control, rodent and other measures to ensure the quality of drugs.
Medical institutions should be stored on a regular basis for the maintenance of medicines. Article XIII of the medical institutions to deploy drugs, packaging materials, containers, and the working environment, should meet the hygiene requirements, to prevent contamination of drugs.
Medical institutions need to deploy drugs on the original minimum packaging of drugs, zero, should be a good record of zero, and retain the original minimum packaging and drug instructions until the end of the sale. The surface of the packaging of the drugs after the split, should indicate the name of the drug, specifications, usage, dosage, expiration date and other content. Article XIV of the hospital category of medical institutions approved preparation of Chinese medicinal preparations, approved by the provincial people's government food and drug supervision and management department, can be entrusted to the drug manufacturer or a "preparation license" of the preparation room of the medical institution preparation. Article XV of the internal departments of medical institutions shall not set up a private pharmacy, medical personnel of medical institutions shall not sell drugs and preparations privately.
Medical institutions shall not use other medical institutions without approval of the preparation. Article 16 Medical institutions shall not use counterfeit or inferior medicines.
Medical institutions in the use of drugs found in the process of counterfeit drugs, substandard drugs, shall immediately stop using, and promptly report to the local food and drug supervision and management department, shall not be disposed of without authorization.
Medical institutions found that the quality of drugs suspect, should be suspended, and at the same time sent to the drug testing organizations; test to determine the counterfeit drugs, substandard drugs, should be promptly reported to the local food and drug supervision and management departments.