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我区卫生厅为贯彻执行《药品管理法》,加强药品监督检验工作,确保药品质量,防止药品生产企业的不合格药品出厂和药品经营企业、医疗单位销售、使用伪劣药品,切实把好药品在产、供、用各环节上的质量关,保障人民用药安全有效,制定了“关于加强药品监督检验工作的暂行规定”.(一)药品生产、经营、使用单位向国家药品监督检验机构实行药品定期报验制度.1.药品生产企业、药品经营企业(包括个体药店)和医疗单位(包括个体诊所),对本单位存放的外观检查质量可疑的药品和生产后存放满五年以上的药品(不包括有保存期、有效期规定的药品和中药材)必须向药品检验所报验.
In order to implement the “Drug Administration Law”, our district health department should step up drug supervision and inspection, ensure the quality of medicines, prevent the unqualified pharmaceutical manufacturers from leaving the factory and the pharmaceutical enterprises and medical units to sell and use counterfeit medicines, Production, supply and use of various links on the quality of the people to ensure safe and effective drug use, developed the “Provisional Regulations on Strengthening Drug Surveillance and Inspection.” (A) drug production, management, use of drugs to the State Drug Administration agencies Periodic inspection system 1. Pharmaceutical manufacturers, pharmaceutical enterprises (including individual pharmacies) and medical units (including individual clinics) shall inspect the quality of the drugs stored in the store for inspection of the quality and the medicines stored for more than five years after manufacture Including the shelf life, the validity of the provisions of the medicines and Chinese herbal medicines) must be submitted to the drug inspection.