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《GMP英语词汇及缩写》
第一部分
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 Ingrediet) 原料药 又称：活性药物组分 AirLock 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；Consignmecnt（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
第二部分 GMP文件常见缩写
ABPI Association of the British Pharmaceutical Industry ADR Adverse Drug Reaction AE Adverse 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 Research Associate CRF Case Report Form
CRO Contract Research Organisation CTA Clinical Trial Application CTC Clinical Trial Certificate CTD Common Technical Document CTX Clinical Trials Exemption DDD Defined Daily Dose 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 Licence 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 Assessment 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 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 Harmonisation IDMC Independent Data-Monitoring Committee IEC Independent Ethics Committee IND Investigational New Drug
INN International Non-proprietary Name International Conference on Harmonisation (ICH) IPC In Process Control IRB Institutional Review Board LICENCE HOLDER MA Marketing Authorisation
MAA Marketing Authorisation Application MAA上市申请
MAH Marketing Authorisation Holder