[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"$fjiDUowtaIEt-4l0FVsYkypACZ9GL2X9ru-VVNYiP6ns":3},{"answer":4,"createTime":5,"id":6,"options":7,"origin":12,"question":19,"related":20,"source":24,"type":25},[],"2024-12-09 12:46:07",169826522,[8,9,10,11],"已批准上市药品的未注册规格,按照药品GMP要求生产的药品可以出口","短缺药品,国务院一律禁止出口","未在我国注册,按照药品GMP要求生产,且符合与我国有相关协议的国际组织要求的药品可以出口","我国境内已经批准上市的药品可以出口",{"count":13,"courseId":14,"courseImg":15,"courseName":16,"workId":17,"workName":18},143,"64b7328c362f8a93a651b6066eb7a3dd","https:\u002F\u002Ftihai-oss-cloud.itihey.com\u002Fimg\u002F172ac4a7c06c96a1b99247f178f85d9c.jpg","药事管理与法规","work_39015800","药品经营管理(执业药师)","下列关于出口药品管理的说法,错误的是",[21,26,36,46,56,65,74,83,92,101],{"answer":22,"createTime":5,"id":6,"options":23,"question":19,"source":24,"type":25},[],[8,9,10,11],"v1",0,{"answer":27,"createTime":28,"id":29,"options":30,"question":35,"source":24,"type":25},[],"2024-12-09 12:46:08",169826523,[31,32,33,34],"药品说明书单色印刷时,专有标识下方必须标示"甲类"或"乙类"字样","药品的使用说明书和大包装的非处方药专有标识不可以单色印刷","非处方药专有标识与药品标签应一体化印刷","非处方药的标签和说明书应经过国家药品监督管理部门的批准","关于非处方药专有标识及其印刷要求的说法,错误的是",{"answer":37,"createTime":38,"id":39,"options":40,"question":45,"source":24,"type":25},[],"2025-01-11 18:38:03",169826524,[41,42,43,44],"拆零药品集中存放于拆零专柜或专区","处方药和非处方药分区存放","含麻黄碱类复方制剂的非处方药开架陈列","中药饮片的柜斗谱书写必须正名正字","根据《药品经营质量管理规范》,关于药品零售企业陈列药品的做法,错误的是",{"answer":47,"createTime":48,"id":49,"options":50,"question":55,"source":24,"type":25},[],"2025-01-11 18:38:04",169826525,[51,52,53,54],"储存疫苗的企业应配备两个以上独立冷库","应当配备冷藏车及车载冷藏箱或保温箱","应当配备冷库制冷设备的双回路供电系统或备用发电机组","应当配备用于冷库温度人工监测、显示、记录、调控及报警的设备","根据《药品经营质量管理规范》,下列关于药品批发企业冷藏冷冻设备的说法,错误的是",{"answer":57,"createTime":48,"id":58,"options":59,"question":64,"source":24,"type":25},[],169826526,[60,61,62,63],"盐酸伪麻黄碱原料药","丁丙诺啡透皮贴剂","所有的抗菌药物","注射用A型肉毒毒素","不得通过互联网销售的药品不包括",{"answer":66,"createTime":28,"id":67,"options":68,"question":73,"source":24,"type":25},[],169826527,[69,70,71,72],"药品名称、数量、价格、批号、规格、生产厂商","供货单位名称、药品名称、数量、价格、生产厂商、规格","供货单位名称、药品名称、数量、价格、批号、生产厂商","供货单位名称、购货单位、数量、价格、批号、规格、生产厂商","根据《药品经营质量管理规范》,药品零售企业销售药品时,开具的销售凭证内容至少应列明",{"answer":75,"createTime":38,"id":76,"options":77,"question":82,"source":24,"type":25},[],169826528,[78,79,80,81],"中成药上市许可持有人","中药生产企业","使用中药饮片的中医医院","具有中药材经营范围的药品批发企业","中国境内不属于可以进口中药材的单位是",{"answer":84,"createTime":48,"id":85,"options":86,"question":91,"source":24,"type":25},[],169826529,[87,88,89,90],"注销乙药店的药品经营许可证","按变更药品经营许可证要求办理相关变更","重新办理甲企业药品经营许可证","重新办理乙药店的药品经营许可证","甲企业为一家药品零售连锁企业,最近几年发展快速,门店数量增长迅速,今日又收购一家单体药店乙,甲收购乙药店后乙药店经营地址和经营范围未发生变化,应",{"answer":93,"createTime":48,"id":94,"options":95,"question":100,"source":24,"type":25},[],169826531,[96,97,98,99],"销售含兴奋剂类药品时,因药品说明书和标签中注明"运动员慎用",所以一律不得向运动员销售","销售第二类精神药品时,若不确定个人消费者是否为成年人,可查验其身份证信息","药学服务人员可向个人消费者合理推荐非处方药","销售含特殊药品复方制剂时,应当登记个人消费者身份证信息","关于药品零售的经营行为管理要求,错误的是",{"answer":102,"createTime":28,"id":103,"options":104,"question":109,"source":24,"type":25},[],169826532,[105,106,107,108],"非首次进口的中药材","首次在中国境内销售的药品","国家药品监督管理局规定的生物制品","从境外进入保税仓库、保税区、出口加工区的药品","下列属于可免予办理进口备案和口岸检验的情形是"]