常用药品监管英语与缩略语

1、常用药品监管英语与缩略语常用药品监管英语与缩略语浙江省药品监督管理局政策法规处一、监管英语1. 中华人民共和国药品管理法Drug Control Law of the People's Republic of China2. 药品生产企业管理control over drug manufacturers3. 药品经营企业管理control over drug distributors4. 医疗机构的药剂管理control over medicines in medical institutions5. 药品管理control over drugs6. 药品包装的管理control ov

2、er drug packaging7. 药品价格和广告的管理control over drug price and advertisement8. 药品监督inspection of drugs9. 法律责任legal liabilities10. 药品标识labels or marks of the drugs11. 假药counterfeit drugs112. 劣药inferior drugs13. 药品检验机构drug quality control laboratory14. 药品的生产企业drug manufacturers15. 经营企业drug distributors16.

3、医疗机构medical institutions17. 药品监督管理部门drug regulatory agency18. 药品批准证明文件drug approval documents19. 行政处分administrative sanctions20. 刑事责任criminal liabilities21. 药品生产质量管理规范Good Manufacturing Practice for Pharmaceutical Products (GMP)22. 药品经营质量管理规范Good Supply Practice for Pharmaceutical Products (GSP)23.

4、药品生产许可证Drug Manufacturing Certificate224. 药品经营许可证Drug Supply Certificate25. 医疗机构制剂许可证Pharmaceutical Preparation Certificate for Medical Institution26. 进口药品注册证书Import Drug License27. 临床试验clinical trial28. 新药证书New Drug Certificate29. 药品批准文号Drug Approval Number30. 在中华人民共和国境内从事药品的研制、生产、经营、使用和监督管理的单位或者个人

5、必须遵守中华人民共和国药品管理法All institutions or individuals engaged in research, production, distribution, use, and administration and supervision of drugs in the People's Republic of China shall abide by drug control law of the people's republic of China.31. 国务院药品监督管理部门主管全国药品监督管理工作。The drug regulatory

6、agency of the State Council shall be responsible for drug administration and supervision nationwide.32. 省、自治区、直辖市人民政府药品监督管理部门负责本行政区域内的药品监督管理工作。The drug regulatory agencies of the governments of provinces, autonomous regions, and municipalities directly under the Central Government shall be responsib

7、le for drug regulation in their administrative areas.33. 药品监督管理部门设置或者确定的药品检验机构承担依法实施药品审批和药品质量监督检查所需的药品检验工作。The drug quality control laboratories established or designated by drug regulatory agencies shall undertake the responsibility for drug testing required for conducting3drug review and approval

8、and controlling drug quality pursuant to the law.34. 开办药品生产企业须经企业所在地省、自治区、直辖市人民政府药品监 督管理部门批准并发给药品生产许可证凭药品生产许可证到工商行 政管理部门办理登记注册。Any newly established pharmaceutical manufacturer shall be subject to approval by the local drug regulatory agency of the government of the province, autonomous region or mu

9、nicipality directly under the Central Government and be granted the Drug Manufacturing Certificate, and, withthe certificate, the manufacturer shall be registered with the administrative agency for industry and commerce.35. 药品生产许可证应当标明有效期和生产范围到期重新审查发证。The term of validation and the scope of manufact

10、uring shall be notedin the Drug Manufacturing Certificate. For renewal of the certificate on expiration, reviewing and approval again is required.药品监督管理部门批准开办药品生产企业应当符合国家制定的药品行业36.发展规划和产业政策防止重复建设。When giving approval to the newly-established manufacturer, the drugregulatory agency shall see to it th

11、at the development programs and policies set by the State for the pharmaceutical industry shall be complied with so as to prevent duplicate construction.37. 开办药品生产企业必须具备以下条件：，一，具有依法经过资格认定的药学技术人员、工程技术人员及相应的技术工人, 二 , 具有与其药品生产相适应的厂房、设施和卫生环境, 三 , 具有能对所生产药品进行质量管理和质量检验的机构、人员以及必要的仪器设备, 四 , 具有保证药品质量的规章制度。An

12、y drug manufacturer to be established shall meet the followingrequirements: (1) stuffed with legally qualified pharmaceutical andengineering professionals and the necessary technical workers;(2)provided with the premises, facilities, and clear environment requiredfor drug manufacturing; (3) having q

13、uality management and control units and personnel capable of quality management of and testing for drugs tobe produced and the necessary instruments and equipment; and (4) establishing rules and regulations to govern the quality of drugs.38. 药品生产企业必须按照国务院药品监督管理部门依据本法制定的药品生产质量管理规范组织生产。药品监督管理部门按照规定对药品

14、生产企业是否符合药品生产质量管理规范的要求进行认证，对认证合格的发给认 4证证书。Drug manufacturers shall conduct production according to the Good Manufacturing Practice Products (GMP) formulated by the drug regulatory agency of the State Council based on this Law. The drug regulatory agency shall inspect a drug manufacturer as to its com

15、pliance with the GMP requirements and issue a certificate to the manufacturer passing the inspection.39. 除中药饮片的炮制外药品必须按照国家药品标准和国务院药品监督管理 部门批准的生产工艺进行生产生产记录必须完整准确。With the exception of the processing of prepared slices of Chinese crude drugs, a drug shall be produced in conformity with the National Dr

16、ug Standard and with the production processes approved by the drug regulatory agency of the State Council, and the production records shall be complete and accurate.40. 药品生产企业改变影响药品质量的生产工艺的必须报原批准部门审核批准。When drug manufacturers make any change in the production process that may affect the drug quality

17、, they shall submit the change to the original authority for reviewing and approval.41. 生产药品所需的原料、辅料必须符合药用要求。Active pharmaceutical ingredients (API) and recipients for the manufacture of pharmaceutical products shall meet the requirements for medicinal use.42. 药品生产企业必须对其生产的药品进行质量检验。Drug manufacturer

18、s shall perform quality test of their products.43. 不符合国家药品标准或者不按照省、自治区、直辖市人民政府药品监督管理部门制定的中药饮片炮制规范炮制的不得出厂。No products that do not meet the National Drug Standards or that are not produced according to the processing procedures for the prepared slices of Chinese crude drugs formulated by the drug regu

19、latory agency of the government of a province, autonomous region, or municipality directly under the Central Government may be released.44. 经国务院药品监督管理部门或者国务院药品监督管理部门授权的省、自治区、直辖市人民政府药品监督管理部门批准药品生产企业可以接受委托生 产药品。A drug manufacturer may not accept any contract production of drugs unless it is5approved b

20、y the drug regulatory agency of the State Council, or bythe drug regulatory agency of the government of a province, autonomous region, or municipality directly under the Central Government authorized by the drug regulatory agency of the State Council.45. 开办药品批发企业须经企业所在地省、自治区、直辖市人民政府药品监 督管理部门批准并发给药品经

21、营许可证.Any newly established drug wholesaler shall be subject to approvalof the local drug agency of the government of the province, autonomous region or municipality directly under the Central Government and be granted the Drug Supply Certificate.46. 开办药品零售企业须经企业所在地县级以上地方药品监督管理部门批准 并发给药品经营许可证。Any new

22、ly established drug retailer shall be subject to approval andbe granted the above certificate by the local drug regulatory agency at or above the county level.47. 药品批发、零售企业凭药品经营许可证到工商行政管理部门办理登记注册。With the Drug Supply Certificate , the wholesaler and the retailer shall be registered with the administ

23、rative agency for industry and commerce.47 .无药品经营许可证的不得经营药品。No one is permitted to distribute drugs without the certificate.48 .药品经营许可证应当标明有效期和经营范围到期重新审查发证。The valid period and the scope of business shall be indicated in theDrug Supply Certificate. For renewal of the certificate upon expiration, rev

24、iewing and approval again is required.49 . 开办药品经营企业必须具备以下条件: , 一 , 具有依法经过资格认定的药学技术人员, 二 , 具有与所经营药品相适应的营业场所、设备、仓储设施、卫生环境, 三 , 具有与所经营药品相适应的质量管理机构或者人员, 四 ,具有保证所经营药品质量的规章制度。A drug distributor to be established shall meet the following requirements:(1) staffed with legally qualified pharmaceutical profes

25、sionals;(2) provided with the business operation premises, equipment, warehouses, and clear environment required for drug distribution;(3) having the quality control units or personnel adaptable the drugs to be distributed; and(4) establishing rules and regulations to govern the quality of the drugs

26、 to be distributed.650 . 药品经营企业必须按照国务院药品监督管理部门依据本法制定的药品经 营质量管理规范经营药品。Drug distributors shall conduct business according to the Good Supply Practice for Pharmaceutical Products (GSP) set by the drug regulatory agency of the State Council based on this Law.药品监督管理部门按照规定对药品经营企业是否符合药品经营质量管理51.规范的要求进行认证，对

27、认证合格的发给认证证书。The drug regulatory agency inspect a drug distributor as to its compliance with the GSP requirements, and issue a certificate to the distributor passing the inspection.52 .药品经营企业购进药品必须建立并执行进货检查验收制度验明药品合 格证明和其他标识，不符合规定要求的不得购进。After receiving the drug purchased, drug distributors shall pas

28、s the established examination and acceptance system, and check the certificate of drug quality, labels and others marks; no drugs that fail to meet the requirements are permitted to be purchased.53 .药品经营企业购销药品必须有真实完整的购销记录。Drug distributors shall keep a real and perfect records of purchasing and sell

29、ing drugs.54 . 购销记录必须注明药品的通用名称、剂型、规格、批号、有效期、生产厂商、购 , 销 , 货单位、购, 销 , 货数量、购销价格、购, 销 , 货日期及国务院药品监督管理部门规定的其他内容。In the record shall be indicated the adopted name of drugs, dosage form, strength or size, batch number, date of expiry, manufacturer, purchaser (or seller), amount of the drug purchased (or so

30、ld), purchase or selling price, date of purchase (or sale) , and other items specified by the drug regulatory agency of the State Council.55 .药品经营企业销售中药材必须标明产地。Drug distributors shall indicate the habitat of Chinese crude drugs to be sold.56 .药品经营企业必须制定和执行药品保管制度采取必要的冷藏、防冻、防 潮、防虫、防鼠等措施保证药品质量。A drug d

31、istributor shall pass the established system for drug storage, and take necessary measures to ensure drug quality, such as cold storing, protecting from being frozen and moisture and guarding against insects and rodents.57 . 药品入库和出库必须执行检查制度。An examination system shall be followed for storing drugs i

32、n warehouse and releasing them from warehouse.58 .城乡集市贸易市场可以出售中药材国务院另有规定的除外。Chinese crude drugs may be sold at fairs in urban and rural areas, except those otherwise specified by the State Council.59 .城乡集市贸易市场不得出售中药材以外的药品但持有药品经营许可证的药品零售企业在规定的范围内可以在城乡集市贸易市场设点出售中药材以外的药品。No drugs other than the Chinese

33、 crude drugs may be sold at fairs inurban and rural areas, but drug retailers holding the Drug SupplyCertificate may, within the specified business scope, sell such drugs at the stores they set up at the fairs.60 .医疗机构配制制剂须经所在地省、自治区、直辖市人民政府卫生行政部 门审核同意由省、自治区、直辖市人民政府药品监督管理部门批准发给医疗机构制剂许可证。Dispensing ph

34、armaceutical preparations by a medical institutionshall be subject to reviewing and permission by the healthadministration agency of the government of the province, autonomous region or municipality directly under the Central Government, and upon approval by the drug regulatory agency of the governm

35、ent. APharmaceutical Preparation Certificate for Medical Institution shall be issued by the above drug regulatory agency.61 .无医疗机构制剂许可证的医疗机构不得配制制剂。No medical institution is permitted to dispense pharmaceutical preparations without the Pharmaceutical Preparation Certificate for Medical Institution.62

36、 .医疗机构制剂许可证应当标明有效期到期重新审查发证。The term of validation shall be noted in the PharmaceuticalPreparation Certificate for Medical Institution. For renewal of the certificate upon expiration, reviewing and approval again is required.63 .医疗机构配制的制剂应当是本单位临床需要而市场上没有供应的品种 并须经所在地省、自治区、直辖市人民政府药品监督管理部门批准后方可配制。The ph

37、armaceutical preparations to be dispensed by the medical institution shall be8those satisfying the clinic need of the institution but not available on the market. It shall be subject to approval in advance by the local drug regulatory agency of the government of the province, autonomous region or mu

38、nicipality directly under the Central Government.64 .医疗机构配制的制剂不得在市场销售。No pharmaceutical preparations dispensed by medical institutions are permitted to be marketed.65.研制新药必须按照国务院药品监督管理部门的规定如实报送研制方法、 质量指标、药理及毒理试验结果等有关资料和样品经国务院药品监督管理 部门批准后方可进行临床试验。A full description of a new drug research and developm

39、ent includingthe manufacturing process, quality specifications, results ofpharmacological and toxicological study, and the related data as well as the samples shall, in accordance with the regulations of the drug regulatory agency of the State Council, be truthfully submitted to the above agency for

40、 reviewing and approval.66. 完成临床试验并通过审批的新药由国务院药品监督管理部门批准发给 新药证书。When a new drug has gone through clinical trials and passed the reviewing, a New Drug Certificate shall be issued upon approval by the drug regulatory agency of the State Council.67. 药物的非临床安全性评价研究机构和临床试验机构必须分别执行药物非临床研究质量管理规范、药物临床试验质量管理规

41、范。The institutions for non-clinical safety evaluation and study andfor clinical study institutions shall respectively follow the GoodLaboratory Practice for Non-Clinical Laboratory Studies (GLP) and Good Clinical Practice (GCP).68. 生产新药或者已有国家标准的药品的须经国务院药品监督管理部门批 准并发给药品批准文号，但是生产没有实施批准文号管理的中药材和中 药饮片除外

42、。Production of a new drug or production of a drug complying withNational Drug Standards shall be subject to the approval by the drug regulatory agency of the State Council, and a drug approval number shallbe issued for it, with the exception of the Chinese crude drugs and the prepared slices of Chin

43、ese crude drugs in which no control by approval number is exercised.69. 实施批准文号管理的中药材、中药饮片品种目录由国务院药品监督管理部9门会同国务院中医药管理部门制定。The list of the Chinese crude drugs and the prepared slices of theChinese crude drugs to be controlled by the approval number shall be compiled by the drug regulatory agency of th

44、e State Council, jointly with the administrative agency for traditional Chinese medicines of the State Council.70. 药品生产企业在取得药品批准文号后方可生产该药品。A drug manufacturer is permitted to produce the drug only after an approval number has been granted to it.71. 药品必须符合国家药品标准。Drugs shall comply with the National D

45、rug Standards.72. 国务院药品监督管理部门颁布的中华人民共和国药典和药品标准为国 家药品标准。The Pharmacopoeia of the People's Republic of China and the Drug Standards issued by the drug regulatory agency of the State Council shall serve as the National Drug Standards.73. 国务院药品监督管理部门组织药典委员会负责国家药品标准的制定和修订。The drug regulatory agency o

46、f the State Council shall organize a pharmacopoeia commission, which shall be responsible for formulating and revising the National Drug Standards.74. 国务院药品监督管理部门的药品检验机构负责标定国家药品标准品、对照品。The drug control institution affiliated to the drug regulatory agency of the State Council is responsible for stand

47、ardizing the National Drug Standard Substance and Reference Substance.75. 药品生产企业、药品经营企业、医疗机构必须从具有药品生产、经营资格的企业购进药品，但是购进没有实施批准文号管理的中药材除外。Drug manufacturers, drug distributors and medical institutions shall purchase drugs from pharmaceutical enterprises, which are qualified for production and distribut

48、ion, with the exception of the Chinese crude drugs in which no control by approval number is exercised.76. 国家对麻醉药品、精神药品、医疗用毒性药品、放射性药品实行特殊管10理。The State exercises special control over narcotic drugs, psychotropic substances, toxic drugs for medical use and radioactive pharmaceuticals.77. 国家实行中药品种保护制度

49、。The State adopts a protection system for certain traditional Chinese medicines.78. 国家对药品实行处方药与非处方药分类管理制度。The State adopts a system of classified management for prescription and non-prescription drugs.79. 药品进口须经国务院药品监督管理部门组织审查经审查确认符合质量 标准、安全有效的方可批准进口并发给进口药品注册证书。Reviewing the drugs to be imported sha

50、ll come of the jurisdiction ofthe drug regulatory agency of the State Council. A drug is permitted to be imported only upon approval granted after confirming that it conforms to the quality, safely and efficiency through examination, and a drug importation license shall be issued.80. 国家实行药品储备制度。The

51、State adopts a policy for drug storage for future use.81. 国内发生重大灾情、疫情及其他突发事件时国务院规定的部门可以紧急 调用企业药品。When major disasters, epidemic situations or other emergencies occur in the country, the department designated by the State Council may allocate drugs from the enterprises to meet the urgent need.82. 禁止生

52、产, 包括配制 , 、销售假药。Production (including dispensing) and distribution of counterfeitdrugs are prohibited.83. 有下列情形之一的为假药：A drug falling into the following categories is deemed as a counterfeit drug: , 一 , 药品所含成份与国家药品标准规定的成份不符的,The ingredients in the drug are different from those specified by the Nation

53、al Drug Standards;, 二 , 以非药品冒充药品或者以他种药品冒充此种药品的。It is not the same drug which is claimed by its name or in reality it is not a drug at11all.84 .有下列情形之一的药品按假药论处：A drug falling into the following categories shall be deemed as a counterfeit drug: , 一 , 国务院药品监督管理部门规定禁止使用的,It s use is prohibited by the pr

54、ovisions of the drug regulatoryagency of the StateCouncil;,二,依照本法必须批准而未经批准生产、进口或者依照本法必须检验而未经检验即销售的,It is produced or imported without approval, or marketed withoutbeing tested, as required by the Law;, 三 , 变质的 ,It is deteriorated;, 四 , 被污染的,It is contaminated;, 五 , 使用依照本法必须取得批准文号而未取得批准文号的原料药生产的It is

55、 produced by using active pharmaceutical ingredients without approval number as required by this Law;, 六 , 所标明的适应症或者功能主治超出规定范围的。The indications or functions indicated are beyond the specified scope.85 . 禁止生产、销售劣药。Production and distribution of drugs of inferior quality are prohibited.86 .药品成份的含量不符合国

56、家药品标准的为劣药。A drug with content not up to the National Drug Standards is a drug of inferior quality.87.有下列情形之一的药品按劣药论处：A drug falling into the following categories shall be deemed as a drug of inferior quality:, 一 , 未标明有效期或者更改有效期的,The date of expiry is not indicated or is altered;, 二 , 不注明或者更改生产批号的,Th

57、e batch number is not indicated or is altered;, 三 , 超过有效期的,It is beyond the date of expiry;, 四 , 直接接触药品的包装材料和容器未经批准的,12No approval certificate is obtained for the immediate packaging material or container;, 五 , 擅自添加着色剂、防腐剂、香料、矫味剂及辅料的,Colorants, preservatives, spices, flavorings, or other recipients have been added without authorization; or, 六 , 其他不符合药品标准规定的。Other cases where the drug standards are not complied with.88. 列入国家药品标准的药品名称为药品通用名称。已经作为药品通用名称的该名称不得作为药品商标使用。A drug name listed in the National Drug Standards is an adopted na