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日前,本刊记者从卫生部获悉,为进一步贯彻执行《药品管理法》,落实《国务院办公厅关于继续整顿和规范药品生产经营秩序加强药品管理工作的通知》精神,根据1998年全国药品抽验计划要求,中国药品生物制品检定所组织各省级药品检验所在全国范围内对部分药品生产、经营、使用部门进行抽样检验,共计93个生产单位生产的82个品种的药品、211个生产批号,检验结果如下:
Recently, this reporter learned from the Ministry of Health was informed that in order to further implement the “Drug Administration Law” and implement the “General Office of the State Council on continuing to rectify and regulate the order of the pharmaceutical production and management to strengthen drug management,” the spirit of the 1998 National Drug Testing Program Requirements, the China Pharmaceutical and Biological Products Inspection Organization organized by the provincial-level drug testing laboratories across the country on some of the drug production, management, use of the department sampling, a total of 93 production units of 82 varieties of drugs, 211 production lot number, inspection The result is as follows: