Article 7 Drug business enterprises and use units shall purchase drugs from enterprises that have the qualifications for drug production and operation; however, except for the purchase of Chinese herbal medicines for which the management of approval numbers is not implemented.
Drug manufacturers and wholesalers shall not sell drugs to drug business enterprises and use units that are not legally qualified.
Article VIII Drug business enterprises and use units to purchase drugs, shall obtain and retain sales vouchers and related information as stipulated by the state; for the first time to supply the unit, it shall also obtain the following information stamped with the seal of the supplying unit for archiving:
(1) "Drug Manufacturing License" or "Drug Business License" and a copy of the business license;
(2) "Good Manufacturing Practice for Drugs" or "Good Manufacturing Practice for Drugs" or "Good Manufacturing Practice for Drugs" or "Good Manufacturing Practice for Drugs" or "Good Manufacturing Practice for Drugs" or "Good Manufacturing Practice for Drugs"; (2) the Drug Production Quality Management Standard" or "Drug Business Quality Management Standard" certification and a copy of the approval of the drug documents;
(c) the supply unit drug sales power of attorney;
(d) a copy of the salesperson's valid identification.
Pharmaceutical companies and the use of units in accordance with the provisions of the preceding paragraph of this article retained sales vouchers and information should be kept until more than the expiration date of the drug 1 year, but not less than 3 years.
Article IX drug business enterprises and the use of units to purchase drugs, shall establish and implement the purchase inspection and acceptance system, inspection of drug certificates of conformity and other identification; does not meet the requirements of the regulations, shall not be purchased.
Pharmaceutical enterprises and the use of units purchasing drugs must have a true and complete procurement and acceptance records, procurement and acceptance records should be confirmed by the signature of the acceptance of personnel.
Article 10 of the pharmaceutical production, wholesale enterprises selling drugs, should be issued with the name of the purchasing unit, generic name of the drug, manufacturer, dosage form, specifications, batch number, quantity, price and other content of the sales voucher, and stamped with a seal.
Drug retailers selling drugs should be issued to indicate the name of the drug, manufacturer, quantity, price, batch number and other content of the sales voucher.
Pharmaceutical production and management enterprises selling drugs must have a true and complete sales records.
Article XI of the purchase and acceptance of drugs and sales records, should indicate the generic name of the drug, the manufacturer (Chinese herbal medicine marked origin), 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 purchase and sale of the contents.
Pharmaceutical purchase, acceptance and sales records should be kept until more than the expiration date of 1 year, but not less than 3 years.
Article XII of the drug production, management enterprises and the use of units shall, in accordance with the requirements of the drug standards and instructions, to take appropriate refrigeration, anti-freezing, moisture-proof, light, ventilation, insect-proof, dust-proof, rodent-proof and other measures to store and transport medicines, and the establishment of drug monitoring, maintenance records.
Pharmaceutical production, management enterprises and the use of units can be entrusted with the conditions to ensure the quality and safety of pharmaceutical enterprises to store and transport drugs.
Article XIII of the drug business enterprises and the use of units shall regularly check the stock of drugs, expired, contaminated, deteriorated and other unqualified drugs, shall be registered and destroyed in accordance with relevant regulations.
Article XIV of the drug business enterprises operating non-pharmaceuticals, drugs and non-pharmaceuticals shall be stored and displayed in separate areas and counters, and set up obvious signs.
Article 15 The indications or functions indicated in the instructions and labels of medicines shall not exceed the scope approved by the State Food and Drug Administration.
Non-pharmaceutical instructions, labels and their promotional materials, shall not be related to the indications of drugs or the content of the main functions.
Article XVI of the medical institutions set up a pharmacy, pharmacy or medicine cabinet, should have the appropriate place, equipment, storage facilities, sanitation and other conditions, the specific conditions by the provincial people's government food and drug supervision and management departments and health departments **** with the development and be published.
Article XVII of the use of drugs to provide patients with medicines should be based on the physician's prescription, shall not be open counter self-selection, trial, clinic, charity sales, consulting and other ways to sell or disguise the sale of drugs.