[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"$frEl2LBMRMlfT3SGkKAmQH_3l2neA6CQciDFBUQwjlWo":3},{"answer":4,"createTime":5,"id":6,"options":7,"origin":12,"question":19,"related":20,"source":31,"type":32},[],"2024-06-15 21:02:59",151836275,[8,9,10,11],"至少1年","至少2年","至少3年","至少5年",{"count":13,"courseId":14,"courseImg":15,"courseName":16,"workId":17,"workName":18},57,"6a5a4041581a14ba9db93c8c7714e8ef","https:\u002F\u002Ftihai-oss-cloud.itihey.com\u002Fimg\u002F5c5ae0ec6aa521c7261f76876d18ac64.png","药事管理与法规-2024春季学期","work_35705464","24总复习五","根据现行版《药品经营质量管理规范》,药品批发企业记录及凭证保存的时限应当是( )",[21,33,42,51,61,70,79,88,97,106],{"answer":22,"createTime":23,"id":24,"options":25,"question":30,"source":31,"type":32},[],"2024-06-15 21:02:57",151836257,[26,27,28,29],"每批产品应当检查产量和物料平衡, 确保物料平衡符合设定的限度","不得在同一生产操作间同时进行不同品种和规格药品的生产操作,除非没有发生混淆或交叉污染的可能","在生产的每一阶段,应当保护产品和物料免受微生物和其他污染","每次生产结束后应当进行清场,下次生产不必检查可直接进行生产","下列说法不正确的是( )","v1",0,{"answer":34,"createTime":23,"id":35,"options":36,"question":41,"source":31,"type":32},[],151836258,[37,38,39,40],"质量管理部门","组织机构","质量控制系统","质量保证系统","企业为保证系统有效运行,必须建立的是( )",{"answer":43,"createTime":23,"id":44,"options":45,"question":50,"source":31,"type":32},[],151836260,[46,47,48,49],"委托方","受托方","生产车间","检验人员","应当对受托生产或检验的全过程进行监督的是( )",{"answer":52,"createTime":53,"id":54,"options":55,"question":60,"source":31,"type":32},[],"2024-06-15 21:02:58",151836262,[56,57,58,59],"生产开始到生产结束的过程","研发到出售的过程","产品从最初的研发、上市直至退市的所有阶段","生产到出售","质量风险管理是采用前瞻或回顾的方式,对质量风险进行评估、控制、沟通、审核的系统过程,是在( )",{"answer":62,"createTime":53,"id":63,"options":64,"question":69,"source":31,"type":32},[],151836264,[65,66,67,68],"饮食习惯","健康","人员着装","卫生习惯","人员卫生操作规程内容不包括( )",{"answer":71,"createTime":53,"id":72,"options":73,"question":78,"source":31,"type":32},[],151836266,[74,75,76,77],"空气悬浮粒子数","温湿度","浮游菌","沉降菌","对洁净级别划分不起主要影响的参数是( )",{"answer":80,"createTime":53,"id":81,"options":82,"question":87,"source":31,"type":32},[],151836268,[83,84,85,86],"卡介苗","青霉素类","β-内酰胺类","维生素类","不需采用专用设施和设备生产的品种是( )",{"answer":89,"createTime":5,"id":90,"options":91,"question":96,"source":31,"type":32},[],151836270,[92,93,94,95],"设备经过改造","设备经过重大维修","操作人员更换","设备使用较长时间","不需要对设备进行再确认的是( )",{"answer":98,"createTime":5,"id":99,"options":100,"question":105,"source":31,"type":32},[],151836272,[101,102,103,104],"1年","2年","3年","4年","批生产记录应按批号归档,保存至药品有效期后( )",{"answer":107,"createTime":5,"id":6,"options":108,"question":19,"source":31,"type":32},[],[8,9,10,11]]