[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"$fagaqDuK5sWYOa579eujFtetlrkJwIa-HIszGQXh4mSg":3},{"answer":4,"createTime":5,"id":6,"options":7,"origin":12,"question":16,"related":17,"source":27,"type":28},[],"2026-01-11 16:08:34",309491545,[8,9,10,11],"30%以上3倍以下","1倍以上5倍以下","2万元以上20万以下","10万元以上50万以下",{"courseId":13,"courseImg":14,"courseName":15},"53e1d2ef4961cca8eea3e23969ad2cb9","https:\u002F\u002Ftihai-oss-cloud.itihey.com\u002Fimg\u002F03a579384a6dc297c89809b582fcc767.png","默认课程","生产、销售假药,对法定代表人、主要负责人没收违法行为发生期间自本单位所获收入,并处所获收入( )的罚款",[18,29,38,47,56,63,72,81,86,95],{"answer":19,"createTime":5,"id":20,"options":21,"question":26,"source":27,"type":28},[],309491536,[22,23,24,25],"USP","BP","NF","JP","日本药典简称( )","v1",0,{"answer":30,"createTime":5,"id":31,"options":32,"question":37,"source":27,"type":28},[],309491537,[33,34,35,36],"以他种药品冒充此种药品的","所标明的适应症超出规定范围的","擅自仿制中药保护品种的","被污染的","属于下列( )情形的药品,为劣药",{"answer":39,"createTime":5,"id":40,"options":41,"question":46,"source":27,"type":28},[],309491538,[42,43,44,45],"擅自委托生产药品的","超过有效期的","擅自添加辅料的","变质的","属于下列( )情形的药品,为假药",{"answer":48,"createTime":5,"id":49,"options":50,"question":55,"source":27,"type":28},[],309491539,[51,52,53,54],"评价抽验","注册检验","监督抽验","上市检验","国家药品抽验以( )为主",{"answer":57,"createTime":5,"id":58,"options":59,"question":62,"source":27,"type":28},[],309491540,[60,54,61,51],"抽查检验","仲裁检验","对有质量争议的药品,药监部门规定的药品检验机构进行的中立性质量鉴定称为( )",{"answer":64,"createTime":5,"id":65,"options":66,"question":71,"source":27,"type":28},[],309491541,[67,68,69,70],"5","7","10","15","当事人对药品检验机构的检验结果有异议,可以申请复验.申请时限为自收到药品检验结果之日起( )日内",{"answer":73,"createTime":5,"id":74,"options":75,"question":80,"source":27,"type":28},[],309491542,[76,77,78,79],"药品检验分为取样、检验、记录和报告三个基本程序","对有掺杂、掺假嫌疑的药品,在国家药品标准规定的检验方法和检验项目不能检验时,药品检验机构可以补充抽检验方法和检验项目进行药品检验","被抽检方应当无偿提供抽检样品,不得拒绝","药品抽样必须由2名以上药品监督检查人员实施","关于药品抽查检验说法错误的是( )",{"answer":82,"createTime":5,"id":83,"options":84,"question":85,"source":27,"type":28},[],309491543,[68,69,67,70],"药品质量抽查检验结果公开不当的,应当自确认公开内容不当之日起( )个工作日内,在原公开范围内予以更正",{"answer":87,"createTime":5,"id":88,"options":89,"question":94,"source":27,"type":28},[],309491544,[90,91,92,93],"成品仓库","药用原、辅料或包装材料仓库","药品仓库","营业场所","抽样场所应当由抽样人员根据被抽样单位类型确定.从药品零售环节抽样一般为( )",{"answer":96,"createTime":5,"id":6,"options":97,"question":16,"source":27,"type":28},[],[8,9,10,11]]