制药常见词汇英文对照

制药常见词汇英文对照中文英文中文英文ICH 颗粒granulation国际协调会议原料药GMP Q7A 粒度particle size原料药API 磨粉milling指导原则guideline 微粉micronizingGMP要求GMP requirements 符合要求Meet therequirements纯度purity 执行v implement物料接收receipt of materials 组织机构organisationalstructure生产production 质量相关事物quality relatedactivities包装packaging 偏差deviation重包装repackaging 关键偏差Critical deviations 贴标labelling 评价evaluation重贴标relabelling 药政检查regulatoryinspections质量控制quality control 严重GMP缺陷serious GMPdeficiencies放行release 审核并批准review and approve储存storage 委派delegate销售distribution 拒收reject安全方面safety aspects 包装物和标签packaging andlabelling materials环境保护protection of theenvironment 实验室控制记录laboratory controlrecord国家法律national laws 标准specifications注册registration 主生产文件master productioninstructions人用药human drug 自检internal auditsself-inspections无菌原料药sterile APIs 合同生产商contractmanufacturers消毒sterilization 验证方案和报告validation protocolsand reports当地药政部门local authorities 投诉complaints化学合成chemical synthesis 维护maintaining提取extraction 校正calibrating发酵fermentation 稳定性数据stability data排除exclude 复验/失效日期retest or expiry dates 临床试验clinical trials 存储条件storage conditions起始物料Starting Material 产品质量回顾product qualityreviews结构单元structural fragment 批生产记录production batchrecords供应商supplier 设施premises化学性质chemical properties 设施变更modified facilities 具体分析case-by-case 证实verify关键步骤critical process 纠偏措施corrective actions前面几部early API steps 工艺的稳定性consistency of theprocess最后几部final steps 分析方法analytical methods 纯化purification 稳定性监控计划stability monitoringprogram分离Isolation 人员资格PersonnelQualifications需要书面写下should be specifiedin writing培训记录Records of training人员卫生Personnel Hygiene 微生物总数total microbialcounts顾问Consultants 控制菌objectionableorganisms潜在污染potential 非无菌non-sterilecontamination微生物标准microbiologicalspecifications专用的Dedicated混淆mix-ups 无水Sewage待验quarantine 垃圾Refuse洗涤剂detergent 卫生Sanitation手烘器air driers 书面程序Written procedures 反作用影响adversely affect 设备维护EquipmentMaintenance蒸汽steam 预防性维护preventativemaintenance通风ventilation 集中生产campaignproduction图纸Drawings 清洗媒介cleaning agents空气过滤air filtration 卸disassembling排气exhaust 连续批号successive batches交叉污染cross-contamination 非专用设备Non-dedicatedequipment空气压力air pressure 可接受标准Acceptance criteria 尘埃dust 残留residues微生物microorganisms 清洁程序cleaning procedures 回风recirculate 状态status管道pipework 预先计划established schedule 中间体intermediate 可追踪的traceable排水沟Drains 对有影响had an impact on饮用水potable water 计算机化系统ComputerizedSystems文件系统DocumentationSystem电子格式electronic form修订历史revision histories 电子签名electronic signatures 扩产报告scale-up reports 中间控制in-process controls 技术转化technical transfer 内控检测in-house testing开发历程报告developmenthistory reports中试规模pilot scale保留期限retention periods 历史数据historical data生产工艺规程Master ProductionInstructions不合格Out-of-specification工艺参数process parameters 混批Blending Batches批量batch size 一级对照品primary standard时间限制time limits 杂质概况impurity profile预期产量expected yield 微生物检测microbiological tests 实际产量Actual yield 商业规模commercial scale关键物料critical materials 留样Retention Samples 进厂物料incoming materials 预验证Prospectivevalidation回顾性验证retrospectivevalidation结晶crystallization不少于not less than 回收溶剂recovered solvents 不大于not more than 母液mother liquors摄氏度centigrade 重新加工Reworking兽用Veterinary use 保留时间retention time氢氧化钠sodium hydroxide 拆分溶液Resolution solution 盐酸hydrochloric acid 水分water甲醇methanol 重金属Heavy metal残留溶剂Residual solvents 流动相Mobile phase炽灼残渣Residue on ignition 柱子column含量Assay 容器Container作一个空白对照Perform a blankdetermination剂型dosage form鉴别Identification 规格strength熔点Melting point 适应症proposed indication 熔程Melting range 给药途径route ofadministration干燥失重Loss on drying 辅料Excipient有关物质Related substance 结构式structural formula比旋度Specific rotation 分子式molecular formula无水anhydrous静态at rest动态in operationGMP车间房间名称中英文对照更衣室? Changing Room一更? First Changing Room手消室? Hands Disinfection Room气闸室? Airlock Room洁具室? Cleaning Tools Room清洗室? Cleaning Room模具室? Dies Room内包装室Immediate Package Room安全门? Emergency Door外包清室Outer Package Removing Room 存料间Storage Room of Raw Materials 粉碎室? Pulverizing Room。