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1.卫生部修改《进口药品管理办法》针对进口伪劣药的出现,卫生部对《进口药品管理办法》第18条第2款作了相应修改。修改后的具体内容如下:国内药品生产企业,药品经营企业和医疗单位在采购进口药品时,应向进口单位索取口岸药检所出具的“进口药品检验报告书”或复印件。为承担售后的责任,该复印件必须盖有复印单位的红
1. The Ministry of Health Amends the Measures for the Administration of Imported Drugs In response to the appearance of imported inferior drugs, the Ministry of Health amended Article 18, paragraph 2, of the Measures for the Administration of Imported Drugs accordingly. The revised contents are as follows: When domestic pharmaceutical manufacturers, pharmaceutical enterprises and medical units purchase imported drugs, they should obtain the Import Drug Inspection Report or a photocopy from the import unit issued by the port drug test. To assume the responsibility for after-sales, the photocopies must be covered with the red copy unit