The medical institutions referred to in the preceding paragraph, including hospitals, maternal and child health centers, health centers, sanatoriums, clinics (including individual), clinics (including individual), health centers (rooms), emergency centers (stations), hospitals for the prevention and treatment of disease (station), nursing homes (station), community health service centers (stations) and other diagnostic institutions engaged in disease diagnosis, treatment, health care activities and family planning technical service institutions. Article 3 The provincial people's government drug supervision and management department in charge of the province's medical institutions drug use supervision and management work. Cities, autonomous regions, counties (cities, districts) drug supervision and management department, is responsible for the supervision and management of the use of drugs in medical institutions within the administrative area.
The relevant administrative departments of the people's governments at or above the county level are responsible for the relevant management of the use of drugs in medical institutions within their respective areas of responsibility. Article IV medical institutions must be approved in accordance with the law, 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 pharmacies or medicine cabinets, should have the appropriate place, equipment, storage facilities and sanitation, equipped with the appropriate pharmacy technicians, set up a quality management organization for the use of medicines or quality management personnel, the establishment of the use of medicines management system. Article 6 outpatient clinics, clinics, health centers (rooms), community health service centers (stations) and other medical institutions, shall not be equipped with medicines other than commonly used medicines and emergency medicines. The scope and varieties of commonly used medicines and emergency medicines shall be prescribed by the health administrative department of the provincial people's government in conjunction with the drug supervision and management department of the provincial people's government.
The scope of the use of drugs in family planning technical service organizations should be consistent with the approved scope of services, services, surgical procedures, and shall not use drugs other than those listed in the catalog of basic drugs used in family planning technical service organizations. The basic medication catalog of family planning technical service institutions shall be prescribed by the drug supervision and management 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 listed in Article 6 of these Measures shall not be changed. Need to change, should be notified in writing to the local drug supervision and management departments, health administrative departments or family planning administrative departments. Article VIII of the medical institutions must be from the "drug production license", "drug business license" and business license of the drug production and business enterprises to purchase drugs. Village health office, individual clinics can also be entrusted to the township health center to purchase drugs on behalf of.
Township health centers on behalf of the township village health department, individual clinic procurement of drugs, should hold the village health department, individual clinic issued a letter of entrustment to accept the supervision and inspection of the local drug supervision and management department, shall not be subcontracted to the drug purchasing qualification to individuals or other units, shall not be to the village health department, individual clinic markups on the sale of drugs. Article IX of the medical institutions to purchase drugs, must strictly comply with national regulations, the establishment of purchase inspection and acceptance system, inspection of drug certificates of conformity and other packaging identification; for drugs that do not comply with the provisions of the drugs, shall not be purchased and used. Article X medical institutions must establish a true and complete record of drug purchases. Drug purchase records should have the following contents:
(a) the generic name of the drug, dosage form, specifications, batch number, expiration date;
(b) the number of purchases, the purchase price, the purchase date;
(c) manufacturers, suppliers;
(d) laws, rules and regulations of other content.
Pharmaceutical purchase record retention time shall not be less than three years; drug expiration date of more than three years, save until one year after the expiration date of the drug. Article XI of the medical institutions shall not be mailed, forged prescriptions, counter open shelf self-selection and charity clinics, charity sales, consultation, trial, the name of the exhibition and sale and other ways to operate or disguise the business of drugs. Article XII of the medical institutions must develop and implement the drug storage system, in accordance with the provisions of the quality and safety of drugs classified storage of drugs.
Drugs and non-drugs, internal drugs and external drugs, Chinese herbal medicines, Chinese medicine, dangerous drugs, easy to string drugs and other drugs, shall be stored separately.
Narcotic drugs, a class of psychotropic drugs, toxic drugs for medical use, radioactive drugs, drug rehabilitation drugs, should be stored in a special library or cabinet, double double-locked storage, special account records. Article XIII of the medical institutions to store drugs, should be based on the quality of the drugs required to take refrigeration, anti-freezing, moisture, light, ventilation, fire, insect, rodent and other measures to prevent contamination, deterioration, failure of drugs.
Medical institutions shall take care of the stored medicines, and shall not use expired, expired, eliminated, moldy, insect-infested, deteriorated medicines. Article XIV of the medical institutions to review and dispense prescriptions of pharmaceutical personnel, must be qualified according to law, pharmacy technicians. Dispensing prescriptions must be checked, and shall not be changed without authorization. Pharmacy personnel have contraindications, pregnancy contraindications, contraindications or overdose of the prescription, should refuse to deploy; if necessary, the original prescription issued by the physician to correct or re-signature confirmation, can only be deployed.
The prescription issued by the medical institution, should be kept in accordance with the national preservation period.