洁净厂房词汇中英文对照,大家补充. |
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 备料室 Materials Preparing Room 硬胶室 Hard Capsules Filling Room 软胶室 Soft Capsules Room 制粒干燥室 Granulating and Drying Room 总混间 Blending Room 中间站 Intermediate Station 压片室Tablets Room Compression Room 包衣室 Coating Room 配浆间 Coating Mixture Preparing Room 铝塑包装间Packing Room 传递窗 Transferring Window 外包装室 Outer Packing Room 蒸馏水室 Water Purifying Room 质检室 Quality Control Room 浓配室 Concentrated Solution Room 稀配室 Diluted Solution Room 灌封室Filling and Sealing Room 存瓶室 Ampul Storage Room 洗瓶室 Ampul Cleaning Room 灭菌间 Sterilizing Room 灯检室 Light Inspection Room 粉针室 Lyophilized Sterile Powder Room 冷冻干燥机 Lyophilizer |
项目管理翻译词汇 GMP英语 PIC/S的全称为：Pharmaceutical Inspection Convention/Pharmaceutical Inspection Cooperation Scheme, PIC/S(制药检查草案), 药品检查协会(PIC/S) ,也有人称PIC/S为医药审查会议/合作计划（PIC/S） PIC的权威翻译：药品生产检查相互承认公约 API(Active Pharmaceutical Ingredient) 原料药 又称：活性药物组分 Air Lock 气闸 Authorized Person 授权人 Batch/Lot 批次 Batch Number/Lot-Number 批号；Batch Numbering System 批次编码系统； Batch Records 批记录；Bulk Product 待包装品；Calibration 校正；Clean area洁净区；Consignment（Delivery）托销药品。 FDA（FOOD AND DRUG ADMINISTRATION）：（美国）食品药品管理局 IND（INVESTIGATIONAL NEW DRUG）：临床研究申请（指申报阶段,相对于NDA而言）；研究中的新药（指新药开发阶段，相对于新药而言，即临床前研究结束） NDA（NEW DRUG APPLICATION）：新药申请 ANDA（ABBREVIATED NEW DRUG APPLICATION）：简化新药申请 TREATMENT IND：研究中的新药用于治疗 ABBREVIATED（NEW）DRUG：简化申请的新药 DMF（DRUG MASTER FILE）：药物主文件（持有者为谨慎起见而准备的保密资料，可以 包括一个或多个人用药物在制备、加工、包装和贮存过程中所涉及的设备、生产过程或物 品。只有在DMF持有者或授权代表以授权书的形式授权给FDA，FDA在审查IND、 NDA、ANDA时才能参考其内容） HOLDER：DMF持有者 CFR（CODE OF FEDERAL REGULATION）：（美国）联邦法规 PANEL：专家小组 BATCH PRODUCTION：批量生产；分批生产 BATCH PRODUCTION RECORDS：生产批号记录 POST-OR PRE- MARKET SURVEILLANCE：销售前或销售后监督 INFORMED CONSENT：知情同意（患者对治疗或受试者对医疗试验了解后表示同意接受治疗或试验） PREscriptION DRUG：处方药 OTC DRUG（OVER—THE—COUNTER DRUG）：非处方药 GMP文件常见缩写 ABPI Association of the British Pharmaceutical Industry ADR Adver Drug Reaction AE Adver Event AIM Active Ingredient Manufacturer ANDA Abbreviated New Drug Application ANOVA Analysis of Variance ASM: Active Substance Manufacturer ATC Anatomical Therapeutic Chemical ATX Animal Test Exemption Certificate BAN British Approved Name BIRA British Institute of Regulatory Affairs BNF British National Formulary BP British Pharmacopoeia C of A Certificate of Analysis C of S Certificate of Suitability CENTRE FOR DRUG EVALUATION (CDE) Centre for Pharmaceutical Administration (CPA) CMS Concerned Member State CMS每个成员国 COS Certificate of Suitability CPMP Committee for Proprietary Medicinal Products CRA Clinical Rearch Associate CRF Ca Report Form CRO Contract Rearch Organization CTA Clinical Trial Application CTC Clinical Trial Certificate CTD Common Technical document CTX Clinical Trials Exemption DDD Defined Daily Do DGC Daily Global Comparison DIA Drug Information Association DMF Drug Master File Drug Registration Branch (DR, Product Evaluation & Registration Division, CPA EDQM (European Directorate for the Quality of Medicines) 欧洲联盟药品质量指导委员会 EEA 欧洲经济地区 EGMA European Generics Medicine Association ELA Established Licen Application EMEA European Medicines Evaluation Agency EMEA （European Agency for the Evaluation of Medicinal Products） 欧洲联盟药品评价机构 EP European Pharmacopoeia EPAR European Public Asssment Reports ESRA European Society of Regulatory Affairs European Pharmacopoeia Commission 欧洲药典委员会 FDA FDA Food and Drug Administration Final Evaluation Report (FER) Free Sale Certificates (FSCs) GCP Good Clinical Practice GCP药品临床研究管理规范 泡腾片 GLP Good Laboratory Practice GLP 药品临床前安全性研究质量管理规范 GMP Good Manufacturing Practice GMP 药品生产质量管理规范 GSP药品销售管理规范 Health Sciences Authority (HSA) HSA’s Medicines Advisory Committee (MAC) IB Investigators Brochure ICH International Conference for Harmonization IDMC Independent Data-Monitoring Committee IEC Independent Ethics Committee IND Investigational New Drug INN International Non-proprietary Name International Conference on Harmonization (ICH) IPC In Process Control IRB Institutional Review Board LICENCE HOLDER MA Marketing Authorization MAA Marketing Authorization Application MAA上市申请 MAH Marketing Authorization Holder MAH 销售许可持有者 MCA Medicines Control Agency MHW Ministry of Health and Welfare (Japan) MR Mutual Recognition MRA 美国与欧盟的互认协议 何曾吹落北风中 MRAs (Mutual Recognition Agreements) 互相認證同意 MRFG Mutual Recognition Facilitation Group MRP Mutual Recognition Procedure NAS New Active Substance 梦见造房子NCE New Chemical Entity NDA New Drug Application New Chemical Entities (NCEs) New Drug Applications (NDAs) NSAID Non Steroidal Anti Inflammatory Drug NTA Notice To Applicants OOS Out of Specification OTC Over the Counter PAGB Proprietary Association of Great Britain Ph Eur European Pharmacopoeia PIL Patient Information Leaflet PL Product Licen POM Prescription Only Medicine PRODUCT OWNER PSU Periodic Safety Updates QA Quality Assurance QC Quality Control RAJ Regulatory Affairs Journal RMS Reference Member State RMS相互认可另一成员国 RSD Relative Standard Deviation Rx Prescription Only SAE Serious Adver Event SMF Site Master File SOP Standard Operating Procedure SOP （STANDARD OPERATION PROCEDURE） 标准运作程序 SPC Summary of Product Characteristics Therapeutic Goods Administration (TGA) USP US Pharmacopoeia VMF Veterinary Master File VPC Veterinary Products Committee A．A．A Addition and Amendments 增补和修订 AC Air Conditioner 空调器 ADR Adver Drug Reaction 药物不良反应 AFDO Association of Food and Drug Officials 食品与药品官员协会（美国） ACC Accept 接受涉农 AQL Acceptable Quality Level 合格质量标准 ADNA Abbreviated New Drug Application 简化的新药申请 BOM Bill of Material 物料清单 BPC Bulk pharmaceutical Chemicals 原料药 CBER Center for Biologics Evaluation Rearch 生物制品评价与研究中心 CFU Colony Forming Unit 菌落形成单位 DMF Drug Master File 药品管理档案 CDER Center for Drug Evaluation and Rearch 药物评价与研究中心 CI Corporate Identity (Image) 企业识别（形象） CIP Cleaning in Place 在线清洗 CSI Consumer Safety Inspector 消费者安全调查员 CLP Cleaning Line Procedure 在线清洗程序 DAL Defect Action Level 缺陷作用水平 DEA Drug Enforcement Administration 管制药品管理 DS documentation System 文件系统 FDA Food and Drug Administration 食品与药品管理局（美国） GATT General Agreement on Tariffs and Trade 关贸总协会 GMP Good Manufacturing Practice 药品生质量管理规范 GCP Good Clinical Practice 药品临床实验管理规范 GLP Good Laboratory Practice 实验室管理规范 GSP Good Supply Practice 药品商业质量规范 GRP Good Retail Practice 药品零售业质量管理规范 GAP Good Agriculture Practice 药材生产管理规范 GVP Good Validation Practice 验证管理规范 GUP Good U Practice 药品使用规范 HVAC Heating Ventilation Air Conditioning 空调净化系统 ISO International Organization for Standardization 国际标准化组织 MOU Memorandum of Understanding 谅解备忘录 PF Production File 生产记录用表格 OTC Over the Counter (Drug) 非处方药品 PLA Product Licen Application 产品许可申请 QA Quality Assurance 质量保证 QC Quality Control 质量控制 QMP Quality Management Procedure 质量管理程序 SDA State Drug Administration 国家药品监督管理局 SMP Standard Management Procedure 标准管理程序 SOP Standard Operating Procedure 标准操作程序 TQC Total Quality Control 全面质量管理 USA United States Pharmacopoeia 美国药典 |
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