Article VI of the drug production, operation and use of units shall, in accordance with the scope of production, operation and use approved by law, from the drug production and operation of qualified enterprises to purchase drugs; however, the procurement of Chinese herbal medicines without the implementation of the management of the approval number except.
Drug manufacturers and wholesalers shall not sell drugs to drug production, operation and use units that are not legally qualified.
Article 7 of the drug production, wholesale enterprises to sell drugs, shall issue sales vouchers indicating the name of the purchasing unit, the generic name of the drug, the manufacturer, dosage form, specifications, batch number, quantity, price and other content, and stamped with a seal.
Drug retailers selling prescription drugs and Class A non-prescription drugs, should be issued with sales vouchers indicating the generic name of the drug, quantity, price, batch number and other content.
Article VIII of the drug production, operation and use of drugs purchased by the unit, shall request, retain sales vouchers and related information required by the state; for the first time to its supply of units, it shall also request the following information stamped with the seal of the unit for archiving:
(a) a copy of the drug production license or drug business license and business license;
(b) "Drug Manufacturing Quality Management Standards" or "Drug Administration Quality Management Standards" certification and a copy of the drug approval documents;
(c) the supplier of drug sales power of attorney;
(d) a copy of the salesperson's valid identification;
(e) sales vouchers sample tickets.
Article IX of the drug production, management and use of drugs purchased by the unit shall establish the purchase inspection and acceptance system, and in accordance with state regulations to establish the purchase, acceptance records. Sales of drugs should be established sales records.
Pharmaceutical procurement, acceptance and sales records, should indicate the generic name of the drug, manufacturer, dosage form, specifications, batch number, expiration date, approval number, purchase and sale of units, purchase and sale of quantities, purchase and sale of prices, purchase and sale of the date of content. Drug acceptance records should also indicate the acceptance of the quality of the situation and processing opinions, and acceptance of the signature of the personnel to confirm.
Pharmaceutical procurement, acceptance and sales records should be kept until more than one year of drug expiration date, and not less than three years.
Article X of the pharmaceutical production, operation and use of units and enterprises engaged in pharmaceutical logistics business transportation, storage of drugs should be carried out in accordance with the requirements of the product specification, with the appropriate shade, refrigeration, light, ventilation, anti-freezing, moisture-proof, insect-proof, dust-proof, rodent-proof facilities and other conditions, and temperature, humidity control equipment, and the establishment of drug monitoring, maintenance records.
Article XI of the drug business enterprises operating non-pharmaceuticals, drugs and non-pharmaceuticals should be divided into areas, sub-counter display, and set up obvious signs.
Article XII of the packaging of drugs, labels, instructions and related promotional materials indicated indications or functions, shall not exceed the scope approved by the State Drug Administration.
Non-pharmaceutical products shall not be labeled with the common name of the drug, its instructions, labels and packaging labels shall not be involved in the content of the drug indications or functions.
Article XIII of the medical institutions shall be equipped with and use of essential drugs in accordance with state regulations.
Medical institutions to provide medicines to patients should be based on the unit's physician's prescription. Patients request a paper prescription, medical institutions must provide.
Medical institutions shall not sell or disguise the sale of medicines by mail, open counter self-selection, trial and so on.
Article 14 of the drug use units set up pharmacies or medicine cabinets, shall have the appropriate personnel, premises, equipment, storage facilities, sanitation and other conditions to ensure the safety of patients with medication, and to comply with the relevant competent authorities of the provincial people's government formulated the quality of the use of medicines management standards.
Article XV of the drug retail enterprises and pharmaceutical units dispensing drugs tools, packaging materials, containers and working environment, shall comply with the health and quality and safety requirements of drugs.
Pharmaceutical retailers and pharmaceutical units of the smallest package of drugs to zero, should make a good record of zero, and will be packaged, labeled and instructions to save until the sale or use of drugs is completed. Drugs after the fragmentation of the contents or packaging surface should indicate the generic name of the drug, dosage form, specifications, batch number, usage, dosage, duration of use and other content.
Article XVI of the pharmaceutical production and operation of enterprises to donate drugs, should be provided to the recipient of the drug production or operation license, a copy of the drug approval documents, drug manufacturers or statutory bodies issued by the donation of a copy of the drug test report and the relevant information provided by the state. Other donors who do not have the qualifications for drug production or operation shall provide the donee with legal proof of drug procurement. The donee shall carry out inspection and acceptance in accordance with the provisions of Article 9, and establish acceptance records.
The actual expiration date of the donated drugs shall not be less than six months.
Article XVII of the drug production, operation and use of drugs should be regularly checked on the stock of drugs, drugs affecting the quality of the hidden dangers, should be eliminated in a timely manner; on the expiration date, contamination, deterioration and other unqualified drugs, should be registered, and in accordance with the relevant provisions to be destroyed.