医疗器械注册管理办法(中英文)翻译
医疗器械注册管理办法
Medical Devices Registration Administration Method
总则
Chapter 1 General Provisions
第一条为规范医疗器械的注册管理，保证医疗器械的安全、有效，根据《医疗器械监督管理条例》，制定本办法。
Article 1 To regulate medical device registration management and ensure their safety and effectiveness of medical device, we set down the management measure according to Regulations for the Supervision and Administration of Medical Device.
第二条在中华人民共和国境内销售、使用的医疗器械均应当按照本办法的规定申请注册，未获准注册的医疗器械，不得销售、使用。
Article 2 All the medical device which would like to sell and use within the territory of the People’s Republic of China shall apply for registration complying with this measure. These medical devices which not get China registration approval should be prohibited to sell and use.
第三条医疗器械注册，是指依照法定程序，对拟上市销售、使用的医疗器械的安全性、有效性进行系统评价，以决定是否同意其销售、使用的过程。
Article 3 Medical device registration is the process of doing systemic evaluation of plan-market medical device on their safety and effectiveness, then decide if medical device can be allowed to sell and use.
第四条国家对医疗器械实行分类注册管理。
Article 4 The state shall classify medical devices and administer them based on this classification.
境内第一类医疗器械由设区的市级（食品）药品监督管理机构审查，批准后发给医疗器械注册证书。
Domestic Class I medical devices shall be inspected, approved and granted with a registration certificate by the food drug regulatory authority of the government of the municipalities consisting of districts.
境内第二类医疗器械由省、自治区、直辖市（食品）药品监督管理部门审查，批准后发给医疗器械注册证书。
Domestic Class II medical devices shall be inspected, approved and granted with a registration certificate by the food drug regulatory authorities of provinces, autonomous regions and municipalities directly under the central government.
境内第三类医疗器械由国家食品药品监督管理局审查，批准后发给医疗器械注册证书。Domestic Class III medical device shall be inspected, approved and granted with registration certificate by State Food Drug Administration.
境外医疗器械由国家食品药品监督管理局审查，批准后发给医疗器械注册证书。Imported medical devices shall be inspected, approved and granted with registration certificate by State Food Drug Administration.
台湾、香港、澳门地区医疗器械的注册，除本办法另有规定外，参照境外医疗器械办理。Taiwan, Hongkong and Macao’s medical device registration shall refer to the regulation of imported medical device.
医疗器械注册证书有效期4年。
Medical devices certificate is valid for 4 years.
第五条医疗器械注册证书由国家食品药品监督管理局统一印制，相应内容由审批注册的（食品）药品监督管理部门填写。
Article 5 Medical devices registration certificate shall be pressed by State Food Drug Administration and the content shall be filled in by inspection department of food drug administration.
注册号的编排方式为：
Registration is arranged as the following:
×（×）1(食)药监械（×2）字××××3第×4××5××××6号。其中：
X (X) 1 SFDA (X2) 字××××3第×4××5××××6号
×1 为注册审批部门所在地的简称：
X 1 : Shortened form of registration inspection department ‘s locus
境内第三类医疗器械、境外医疗器械以及台湾、香港、澳门地区的医疗器械为“国”字；“国” is for domestic Class III medical devices, imported medical devices and medical devices of Taiwan, Hongkong and Macao.
境内第二类医疗器械为注册审批部门所在的省、自治区、直辖市简称；
境内第一类医疗器械为注册审批部门所在的省、自治区、直辖市简称加所在设区的市级行政区域的简称，为××1（无相应设区的市级行政区域时，仅为省、自治区、直辖市的简称）；
×2为注册形式（准、进、许）：
“准”字适用于境内医疗器械；
“进”字适用于境外医疗器械；
“许”字适用于台湾、香港、澳门地区的医疗器械；
××××3为批准注册年份；
×4为产品管理类别；
××5为产品品种编码；
××××6为注册流水号。
医疗器械注册证书附有《医疗器械注册登记表》（见本办法附件1），与医疗器械注册证书同时使用。
Medical device registration certificate is attached with medical device registration record, and shall be used along with medical device registration certificate.
第六条生产企业提出医疗器械注册申请，承担相应的法律义务，并在该申请获得批准后持有医疗器械注册证书。
Manufacturers put forward medical device registration application, take relevant regal responsibility and keep medical device registration certificate after getting application approval.
办理医疗器械注册申请事务的人员应当受生产企业委托，并具有相应的专业知识，熟悉医疗器械注册管理的法律、法规、规章和技术要求。
Individuals who do medical device registration application should be authorized by manufacturer, possess professional knowledge, are familiar with medical device registration administration law, regulation, rules and technical requirement.
申请境外医疗器械注册的，境外生产企业应当在中国境内指定机构作为其代理人，代理人应当承担相应的法律责任；并且，境外生产企业应当委托中国境内具有相应资格的法人机构或者委托其在华机构承担医疗器械售后服务。
When doing imported medical devices registration, the overseas manufactures shall authorize an unit to be their agent in Chinese territory and the agent should take relevant legal responsibilities.
Meanwhile overseas manufactures shall authorize qualified body corporate or theirs own organ located in China to do after sales service.
第七条申请注册的医疗器械，应当有适用的产品标准，可以采用国家标准、行业标准
或者制定注册产品标准，但是注册产品标准不得低于国家标准或者行业标准。
Article 7 Medical devices which applying for registration shall have suitable product standard that can adopt state standard, industry standard or edit registration standard, but registration standard should not inferior to state standard or industry standard.
注册产品标准应当依据国家食品药品监督管理局规定的医疗器械标准管理要求编制。Registration standard shall be edited according to medical device standard administration regulation stipulated by state food drug supervision administration.
第八条申请第二类、第三类医疗器械注册，生产企业应当符合国家食品药品监督管理局规定的生产条件或者相关质量体系要求。
Article 8 Applying for Class II and Class III medical device registration, manufacture shall comply with relevant manufacturing condition or quality system requirement stipulated by state food drug supervision administration.
第二章医疗器械注册检测
Chapter 2 Medical devices registration testing
第九条第二类、第三类医疗器械由国家食品药品监督管理局会同国家质量监督检验检疫总局认可的医疗器械检测机构进行注册检测，经检测符合适用的产品标准后，方可用于临床试验或者申请注册。
Article 9 Class II and Class III medical devices shall be tested by medical device testing organization approbated by State Food Drug Supervision Administration and State Quality Supervision Inspection and Quarantine, then can be used in clinical trial or apply for registration.
经国家食品药品监督管理局会同国家质量监督检验检疫总局认可的医疗器械检测机构（以下简称医疗器械检测机构）目录另行发布。
The list of medical device testing organization approbated by State Food Drug Supervision Administration and State Quality Supervision Inspection and Quarantine (medical device testing organization for short in the following) shall be issued at another time.
第十条医疗器械检测机构应当在国家食品药品监督管理局和国家质量监督检验检疫总局认可的检测范围内，依据生产企业申报适用的产品标准（包括适用的国家标准、行业标准或者生产企业制定的注册产品标准）对申报产品进行注册检测，并出具检测报告。
Article 10 Medical device testing organization should do registration testing on applicant products according to available product standard including state standard, industry standard or registration product standards edited by manufacture within the specific testing range approbated by State Food Drug Supervision Administration and State Quality Supervision Inspection and Quarantine.
尚未列入各医疗器械检测机构授检范围的医疗器械，由相应的注册审批部门指定有承检能力的检测单位进行检测。
For the medical device that have not been listed in testing range of all medical device testing organization should be tested by qualified testing united approbated by registration inspection department.
境外医疗器械的注册检测执行《境外医疗器械注册检测规定》。
Imported medical device registration shall perform “Imported Medical Device Registration Testing Regulation”.
第十一条同一注册单元内所检测的产品应当是能够代表本注册单元内其他产品安全性和有效性的典型产品。
Among one testing unit the tested product should be the typical product that can representing the safety and effectiveness of other products.
第十二条同一生产企业使用相同原材料生产的同类产品，如果生产工艺和预期用途保持不变，重新注册时，对产品的生物学评价可以不再进行生物相容性试验。
For re-registration the same kind products which made of same material and manufactured by one manufacturer would not be tested for biological compatibility item during biological evaluation if manufacturing technics and intended use do not change.
同一生产企业使用已经通过生物学评价的原材料生产的同类产品，如果生产工艺保持不变，预期用途保持不变或者没有新增的潜在生物学风险，申请注册时，对产品的生物学评价可以不再进行生物相容性试验。
When register the products which manufactured by one manufacturer, made of same material that have done biological evaluation and do not change their manufacturing technics, intended use and have no new potential biological risk would not be tested for biological compatibility during biological evaluation.
第十三条申请第二类、第三类医疗器械注册，同时满足以下条件的，可以免予注册检测：
Applying for Class II and Class III medical device registration will be exempted of doing registration testing if satisfy the following conditions:（一）所申请注册的医疗器械与本企业已经获准注册的医疗器械的基本原理，主要功能、结构，所用材料、材质，预期用途属于同一类；
Applying medical device and applied medical device is same in the basic principle, main function, structure, material and intended use.
（二）生产企业已经通过医疗器械生产质量管理规范检查或者已经获得医疗器械质量体系认证，并且生产企业能够提供经原企业生产条件审查机构认可的检测报告；
The manufacturers have passed the medical device manufacturing quality
administration regulation testing or get approval of medical device quality system certification, meanwhile the manufacturers can provide the admissive testing report by inspection institution under former manufacturing condition.
（三）所申请注册的医疗器械与本企业已经获准注册并且已经通过注册检测的同类产品比较，未发生涉及安全性、有效性改变，或者虽然涉及安全性、有效性改变，但是改变部分和由其引起产品其他相关安全性、有效性变化的部分都已经通过了医疗器械检测机构检测；Comparing with approved registration medical devices , the same kind of applying medical devices do not have changes concerning safety and effectiveness areas or despite of having changes concerning safety and effectiveness areas which have been tested by medical device testing institution.
（四）已经获准注册的本企业同类产品按照规定进行医疗器械不良事件监测，并且未发现严重不良事件；
The same kind of approved registration medical devices have not been found adverse events in the process of MDR.
（五）已经获准注册的本企业同类产品1年内无（食品）药品监督管理部门产品质量监督抽查不合格记录；
The same kind of approved registration medical devices have not been found ineligible records in the process of product quality selective examination by food drug supervision administration within one year.
（六）境外医疗器械已经通过境外政府医疗器械主管部门的上市批准。
Overseas medical devices have got pre-market approval by overseas medical device supervision government.
第十四条申请第二类、第三类医疗器械产品重新注册，同时满足以下条件的，可以免予注册检测：
Applying for Class II and Class III medical device re-registration will be exempted of doing registration testing if satisfy the following conditions:
（一）申请重新注册的医疗器械与本企业已经获准注册的医疗器械的基本原理，主要功能、结构，所用材料、材质，预期用途属于同一类；
Applying re-registration medical device and applied medical device is same in the basic principle, main function, structure, material and intended use.
（二）生产企业已经通过医疗器械生产质量管理规范检查或者已经获得医疗器械质量体系认证，并且生产企业能够提供经原企业生产条件审查机构认可的检测报告；
The manufacturers have passed the medical device manufacturing quality administration regulation testing or get approval of medical device quality system certification, meanwhile the manufacturers can provide the admissive testing report by inspection institution under former manufacturing condition.
（三）申请重新注册的医疗器械与已经通过注册检测的原注册产品相比较，未发生涉及安全性、有效性改变，或者虽然涉及安全性、有效性改变，但是改变部分和由其引起产品其他相关安全性、有效性变化的部分都已经通过了医疗器械检测机构检测；
Comparing with approved registration medical devices , the same kind of applying re-registration medical devices do not have changes concerning safety and effectiveness areas or despite of having changes concerning safety and effectiveness areas which have been tested by medical device testing institution.
（四）申请重新注册的医疗器械在原医疗器械注册证书有效期内按照规定进行医疗器械不良事件监测，并且未发现不良事件；
Applying for re-registration medical devices have not been found adverse events in the process of MDR within the expiration date of the former medical device certificate.
（五）原注册医疗器械1年内无（食品）药品监督管理部门产品质量监督抽查不合格记录。
The former approved registration medical devices have not been found ineligible records in the process of product quality selective examination by food drug supervision administration within one year.
第十五条已经通过境外政府医疗器械主管部门的上市批准、对安装场地有特殊要求、检测困难的大型医疗器械，可以申请暂缓检测，于取得医疗器械注册证书后再对产品进行补充检测。
Huge medical equipments which have got pre-market notification by overseas medical device supervision department, need special requirements on spot installation and have difficulty for testing can applying for postpone testing can be done supplement testing after getting medical device certificate.
根据前款规定申请暂缓检测而获准注册的产品，生产企业必须在首台医疗器械入境后、投入使用前完成注册检测。经检测合格后方可投入使用。
For the products satisfied with above regulation that get registration approval when applying for postpone testing, the manufacture shall complete registration testing after importing the first medical device, until the testing is eligible the product can be put into use.
第三章医疗器械临床试验
Chapter 3 Medical device clinical trial
第十六条申请第二类、第三类医疗器械注册，应当提交临床试验资料。
When applying for Class II and Class III medical devices registration, clinical trial material should be submitted.
临床试验资料提供方式执行《医疗器械注册临床试验资料分项规定》（见本办法附件12）。
The submission methods of clinical trial material shall comply to ‘Medic al Device Registration on Clinical Trial Material Itemize Regulation’.(Refer to attachment 12)
第十七条在中国境内进行医疗器械临床试验的，应当严格执行《医疗器械临床试验规定》。
The clinical trial processed in China shall strictly comply to ‘Medical Device Clinical Trial Regulation’.
第十八条在中国境内进行临床试验的医疗器械，其临床试验资料中应当包括临床试验合同、临床试验方案、临床试验报告。
The clinical trial material of medical devices processed in China shall include clinical trail agreement, clinical trial project and clinical trial report.
（食品）药品监督管理部门认为必要时，可以要求生产企业提交临床试验须知、知情同意书以及临床试验原始记录。
Food drug supervision administration could ask manufacture to provide clinical trial memorandum, acknowledgment letter and clinical trial original records.
第四章医疗器械注册申请与审批
Chapter 4 Medical device registration application and inspection
第十九条申请医疗器械注册，申请人应当根据医疗器械的分类，向本办法第四条规定的相应（食品）药品监督管理部门提出申请，并应当填写医疗器械注册申请表，按照本办法附件2、附件3、附件6、附件8或者附件9的相应要求提交申请材料。申请材料应当使用中文；根据外文资料翻译的申请材料，应当同时提供原文。
When applying for medical devices registration, applicants shall accord with the
medical device classification and apply to concerning food drug supervision administration according to item 4 of this methods.
申请人提交的医疗器械说明书应当符合《医疗器械说明书、标签和包装标识管理规定》。Medical device user manual submitted by applicants shall accord with ‘Administration Regulation of Medical Device user man ual, labeling and package '.
申请人应当对其申请材料全部内容的真实性负责。
Applicants shall take the responsibility of the truth about the fully application material.
第二十条（食品）药品监督管理部门收到申请后，应当根据下列情况分别作出处理：Food drug supervision administration shall treat respectively depending on the following conditions:
（一）申请事项依法不属于本部门职权范围的，应当即时作出不予受理的决定，并告知申请人向有关行政机关申请；
If application articles legally do not belong to authorized scope of this department, should issue a rejection notice and advance applicants to apply for concerning administration unit.
（二）申请材料存在可以当场更正的错误的，应当允许申请人当场更正；
If there is mistake in the application material that could be correct on-spot, the applicants shall be permitted to correct on spot.
（三）申请材料不齐全或者不符合形式审查要求的，应当当场或者在5个工作日内发给申请人《补正材料通知书》，一次性告知申请人需要补正的全部内容，逾期不告知的，自收到申请材料之日起即为受理；
If the application material is incomplete or not in accord with formal inspection
requirement, please inform applicant on-spot or issue applicant with ‘Supplement Material Notice Letter’ within 5 workdays and inform applica nt all the requested supplementary material at one time. Without informing within appointed period, the material receiving date should be regarded as the acceptance date.
（四）申请材料齐全、符合形式审查要求的，或者申请人按照要求提交全部补正申请材料的，予以受理。
It should be accepted if the application material is complete, accord with formal inspection request or applicants submit all requested supplement material according to the concerning requirements.
（食品）药品监督管理部门受理或者不予受理医疗器械注册申请，应当出具加盖本部门专用印章并注明日期的《受理通知书》或者《不予受理通知书》。
Whatever food drug supervision administration accept medical devices application or not, an acceptance notice or a rejection letter should be issued by department with special seal and date.
第二十一条（食品）药品监督管理部门受理医疗器械注册申请后，应当在本办法第二十二条规定的期限内对申请进行实质性审查并作出是否给予注册的书面决定。经审查符合规定批准注册的，自书面批准决定作出之日起10个工作日内发给医疗器械注册证书。经审查不符合规定的，作出不予注册的书面决定，并说明理由，同时告知申请人享有依法申请行政复议或者提起行政诉讼的权利。
Food drug supervision administration shall do substantiality inspection on application and make a paper decision on whether administer registration according to the stipulated term in item 22 of this method. On the condition that material accords with inspection regulation and administer registration, medical device registration certificates shall be issued within 10 workdays counted from date of the paper approval decision-making.
第二十二条设区的市级（食品）药品监督管理机构应当自受理申请之日起30个工作日内，作出是否给予注册的决定。
Food Drug regulatory authority of the government of the municipalities consisting of districts shall make a division whether to administer registration within 30 workdays from the date of application.
省、自治区、直辖市（食品）药品监督管理部门应当自受理申请之日起60个工作日内，作出是否给予注册的决定。
Food Drug regulatory authorities of the provinces, autonomous regions and municipalities shall make a division whether to administer registration within 60 workdays form the date of application.
国家食品药品监督管理局应当自受理申请之日起90个工作日内，作出是否给予注册的决定。
Food Drug regulatory authority directly under State Council shall make a make a division whether to administer registration within 90 workdays form the date of application.
在对注册申请进行审查的过程中，需要检测、专家评审和听证的，所需时间不计算在本条规定的期限内。（食品）药品监督管理部门应当将所需时间书面告知申请人。
In the process of inspection, if testing, technical review by specialists and audit are needed, the requested time is besides from the regulated period of this article. Food Drug Administration shall inform applicants with paper notice about the needed time.
第二十三条未获得境外医疗器械上市许可的境外医疗器械，申请注册时，参照境内同类产品注册的技术审查要求执行（需要提交的材料见本办法附件8、附件9）。
When apply for registration, the imported medical devices without marketing
permission at overseas shall refer to registration technical inspection requirements of the domestic products in the same kind (the requested submission material shall refer to attachment 8 and attachment 9).
第二十四条（食品）药品监督管理部门在对医疗器械注册申请材料进行技术审查时，需要生产企业补充材料的，应当一次性发出书面补充材料通知。
In the inspection process of medical devices registration application material, SFDA shall issue paper supplementary notice to manufacture at one time if supplementary material is needed.
生产企业应当在60个工作日内按照通知要求将材料一次性补齐，补充材料的时间不计算在（食品）药品监督管理部门进行实质审查的期限内。生产企业未能在规定的时限内补充材料且没有正当理由的，终止审查。
Manufacture shall submit all the requested supplementary material at one time according to requirement within 60 workdays. The additional time can not be counted to the SFDA’s substantial inspection time. Inspection shall be discontinued that manufactures do not supplement the requested material within regulated time and have no allowable reason.
第二十五条注册申请被终止审查的，在被终止审查后的6个月内不得再次申请。
For the discontinued inspection, re-registration should not applied within 6 months from the discontinued date.
第二十六条生产企业对补充材料通知内容有异议的，可以在规定的时限内向（食品）药品监督管理部门提出书面意见，说明理由并提供技术支持材料，经（食品）药品监督管理部门审查后作出决定。
If manufactures have suspicion for the supplementary material notice, a paper suggestion can be advanced to SFDA at limited time, explain excuse and offer
technical supporting material that shall be inspected by SFDA, finally SFDA will give a decision.
第二十七条医疗器械产品的注册单元原则上以技术结构、性能指标和预期用途为划分依据。
Basically the classification basis of medical devices registration unit is technological structure, performance and intended use.
第二十八条作为部件注册的医疗器械，申请人应当说明与该部件配合使用的推荐产品、部件的名称、型号、规格。
For medical devices registered as parts, applicants shall explain the recommended products, parts name, model and specifications to work with them.
已经获准注册的部件组合成的整机，必须履行整机注册手续。
A complete machine combined with all registered parts shall implement complete unit registration procedure.
以整机注册的医疗器械，申请注册时应当列出其主要配置。如果某个主要配置部件性能规格发生改变，整机应当重新注册。
When medical devices registering as a complete unit, its main deployment should be listed. A new re-registration should be requested if the main deployments change their performance and specifications.
以整机注册的医疗器械，其医疗器械注册证书附表中的“产品性能结构及组成”栏内所列出的组合部件在不改变组合形式和预期用途的情况下单独销售的，可以免予单独注册。
If the combination parts which have been registered as a complete unit listed on column ‘performance, structure and components of the product’ of the ‘Medical Device Registration Record ’would be allowed to exempt from sole registration when be sold solely without changing its combination form and intended use.
第二十九条（食品）药品监督管理部门应当在行政机关的网站和医疗器械注册办公场所公示相应的医疗器械注册所需的条件、程序、期限、需要提交的全部材料的目录和申请书示范文本等。
SFDA shall issue the condition, procedure, time limit, all requested material directory, samples of application letters of medical devices registration on administrative website and registration handling area.
第三十条（食品）药品监督管理部门对医疗器械注册申请进行审查时，应当公示审批过程和审批结果。申请人和利害关系人可以对直接关系其重大利益的事项提交书面意见进行陈述和申辩。
SFDA shall issue publicly of the inspection process and result during the inspection process of medical device application. Applicants and persons concerned would submit paper advice to state and excuse for the badly concerned matter.
第三十一条国家食品药品监督管理局应当定期在其政府网站上公布已经获准注册的医疗器械目录，供公众查阅。
SFDA shall regularly issue the approved medical devices list on its government website for public reference.
第三十二条医疗器械注册申请直接涉及申请人与他人之间重大利益关系的，（食品）药品监督管理部门应当告知申请人、利害关系人可以依照法律、法规以及国家食品药品监督管理局的其他规定享有申请听证的权利；在对医疗器械注册申请进行审查时，（食品）药品监督管理部门认为涉及公共利益的重大许可事项，应当向社会公告，并举行听证。
第五章医疗器械的重新注册
Chapter 5 Medical device re-registration
第三十三条医疗器械注册证书有效期届满，需要继续销售或者使用医疗器械的，生产
企业应当在医疗器械注册证书有效期届满前6个月内，申请到期重新注册。逾期办理的，重新注册时应当对产品进行注册检测。
Manufacturers shall re-register medical devices certificates within 6 months before expiration date if they would like to sell or use medical devices with overdue certificates.
第三十四条医疗器械注册证书中下列内容发生变化的，生产企业应当自发生变化之日起30日内申请变更重新注册：
If any content in medical devices certificate listing below has changed, Manufactures shall apply for alteration and re-registration in 30 days from changing.
（一）型号、规格；
Specifications, models
（二）生产地址；
Manufacturing address
（三）产品标准；
Product standards
（四）产品性能结构及组成；
Performance, structure and components of product
（五）产品适用范围。
Indications
第三十五条医疗器械注册证书有效期内，产品管理类别发生改变的，生产企业应当在6个月内，按照改变后的类别到相应的（食品）药品监督管理部门申请变更重新注册。
During medical device certificate validity period, if the administrative catalog changes, manufacturers shall apply for alteration and re-register according to the changed catalog in concerning regulatory authority of the government.
第三十六条申请医疗器械重新注册的，应当填写医疗器械注册申请表，并按照本办法附件4、附件5或者附件7的相应要求向（食品）药品监督管理部门提交申请材料。
When applying for re-registration, shall fill in medical device application form and submit application material requested by this method attachment 4,5 or 7 to SFDA.
重新注册的受理与审批程序，本章没有规定的，适用本办法第四章的相关规定。
If there is no regulation on re-registration acceptance and inspection procedure in this chapter, please refer to chapter 4 regulation.
第三十七条有下列情形之一的医疗器械，不予重新注册：
Re-registration is not allowed for any condition below:
（一）未完成（食品）药品监督管理部门在批准上市时按照国家食品药品监督管理局有关规定提出的要求的；
（二）经国家食品药品监督管理局再评价属于淘汰品种的；
Belong to out of date catalogs when re-evaluated by SFDA.
（三）按照《医疗器械监督管理条例》的规定撤销医疗器械注册证书的。
Medical device certificates that were withdrawed by SFDA.
第六章医疗器械注册证书的变更与补办
Alterating and Supplementing of medical device certificates
第三十八条医疗器械注册证书载明内容发生下列变化的，生产企业应当自发生变化之日起30日内申请医疗器械注册证书变更：
Any content listed in medical device has changed, manufactures shall apply for alteration registration on medical device registration certificates within 30 days from the altering date.
生产企业实体不变，企业名称改变；
Manufacture substantiality does not change, name has been altered.
生产企业注册地址改变；
Manufacture registered address has been altered.
生产地址的文字性改变；
Literal alteration of manufacturing address.
（四）产品名称、商品名称的文字性改变；
Literal alteration of product name and trade name.
（五）型号、规格的文字性改变；
Literal alteration of specifications and models.
（六）产品标准的名称或者代号的文字性改变；
Literal alteration of name or code of product standard.
（七）代理人改变；
Agent changes.
（八）售后服务机构改变。
After sales service changes.
第三十九条申请医疗器械注册证书变更的，应当填写医疗器械注册证书变更申请表，并按照本办法附件10的要求向原注册审批部门提交有关材料和说明。原注册审批部门对申
英汉互译在线翻译怎样实现
现在英语的重要性相信大家都是有所了解的，特别是外贸工作者对英语的重要性更是深有体会的。同时在学业学习的过程中我们也是会经常遇到一些英汉互译的问题的额，那么我们应该怎样在线实现英汉互译的问题呢？下面就一起来看一下吧。 步骤一：要在线实现英汉互译的问题，我们就需要通过浏览器搜索在线翻译，进入下面这个页面来帮助我们进行实现。 步骤二：通过浏览器进入在线翻译页面后，有两个选项一个是短句翻译的选项，中文150字以内，英文150词以内都支持进行翻译，适合零散短句，日常用语，商贸交流，邮件往来，地址信息等短文本的翻译。
步骤三：还有一个选项是文档翻译的选项，一次只支持翻译一个文档，所支持翻译的文档格式有一下几种：PDF、WORD文档中的图片、扫描件、图纸。但是背景模糊的纯图片无法进行翻译。 步骤四：了解完上面的两个选项后，我们就可以根据需要选择一个选项进入了，下面小编就选择短句翻译的选项，来为大家进行讲解。
步骤五：转入短句翻译的选项后，会出现两个文本框，我们需要在左边的文本框中输入需要进行翻译的语句。 步骤六：语句输入好后，在文本框的上方可以对一些翻译的选项设置，这样可以帮助我们更快的实现翻译。
步骤七：翻译选项设置好后，就可以通过选择开始翻译按钮，对短语进行翻译了。 步骤八：耐心等待短语翻译结束后，翻译结果会在右边的文本框中呈现，我们可以通过文本框上方的复制按钮对翻译后的结果进行复制粘贴，也可以直接通过鼠标选中进行复制粘贴。
英汉互译的实现方法，上面已经为大家分享过了，实现过程简单快速，生活中再遇到关于翻译的问题，就可以用这个方法来进行实现了。
医学基本中英文对照
1、颅脑 大脑 cerebrum 大脑纵裂 longitudinal cerebral fissure 大脑皮质 cerebral 大脑镰 falx cerebri 大脑导水管，中脑水管 cerebral aqueduct 中脑 midbrain, mesencephalon 小脑 cerebellum 小脑幕 tentorium cerebelli 丘脑，视丘 thalmus 延髓 medulla oblongata 侧脑室 lateral ventricle 第三脑室 third ventricle 第四脑室 fourth ventricle 第五脑室 fifth ventricle 脑桥，桥脑 pons 脑干 brain stem 间脑 diencephalon 中间块 intermidiate mass 尾状核 caudate nucleus 脉络丛 choroid plexus 胼胝体 corpus callosum 脑岛，岛叶 insula 大脑脚 cerebral peduncles 大脑外侧沟（窝、裂） lateral sulcus , sylvius fissure 穹窿 fornix 透明隔 septum pellucidum 透明隔腔 cavity of septum pellucidum 额叶 frontal lobe 顶叶 parietal lobe 枕叶 occipital lobe 颞叶 temporale lobe 缘叶 limbic lobe 大脑动脉环 Willi's artery circle 大脑前动脉 anterior cerebral artery 大脑中动脉 middle cerebral artery 大脑后动脉 posterior cerebral artery 基底动脉 basilar artery
职称英文翻译
公司企业常见部门名称英文 总公司Head Office 分公司Branch Office 营业部Business Office 人事部Personnel Department (人力资源部)Human Resources Department 总务部General Affairs Department 财务部General Accounting Department 销售部Sales Department 促销部Sales Promotion Department 国际部International Department 出口部Export Department 进口部Import Department 公共关系Public Relations Department 广告部Advertising Department 企划部Planning Department 产品开发部Product Development Department 研发部Research and Development Department(R&D) 秘书室Secretarial Pool 常见职位、职务英文译名 Accounting Assistant会计助理 Accounting Clerk记帐员 Accounting Manager会计部经理 Accounting Stall会计部职员 Accounting Supervisor会计主管 Administration Manager行政经理 Administration Staff行政人员 Administrative Assistant行政助理 Administrative Clerk行政办事员 Advertising Staff广告工作人员 Airlines Sales Representative航空公司定座员 Airlines Staff航空公司职员 Application Engineer应用工程师 Assistant Manager副经理 Bond Analyst证券分析员
英汉互译在线翻译句子
如果只是遇见，不能停留，不如不遇见。 if we can only encounter each other rather than stay with each other,then i wish we had never encountered. 2 。宁愿笑着流泪，也不哭着说后悔。心碎了，还需再补吗？ i would like weeping with the smile rather than repenting with the cry, when my heart is broken, is it needed to fix? 3 。没有谁对不起谁，只有谁不懂得珍惜谁。 no one indebted for others, while many people dont know how to cherish others. 4 。命里有时钟需有命里无时莫强求you will have it if it belongs to you, whereas you dont kvetch for it if it doesnt appear in your life. 5 。当香烟爱上火柴时，就注定受到伤害when a cigarette falls in love with a match, it is destined to be hurt. 6。爱情??在指缝间承诺指缝…。在爱情下交缠。love ,promised between the fingers finger rift, twisted in the love 7。没有人值得你流泪，值得让你这么做的人不会让你哭泣。 no man or woman is worth your tears, and the one who is, won?t make you cry. 8 。记住该记住的，忘记该忘记的。改变能改变的，接受不能改变的。 remember what should be remembered, and forget what should be forgotten. alter what is changeable, and accept what is unchangeable. love is like a butterfly. it goes where it pleases and it pleases where it goes. 爱情就像 一只蝴蝶，它喜欢飞到哪里，就把欢乐带到哪里。 if i had a single flower for every time i think about you, i could walk forever in my garden. 假如每次想起你我都会得到一朵鲜花，那么我将永远在花丛中徜徉。 within you i lose myself, without you i find myself wanting to be lost again. 有了你，我迷失了自我。失去你，我多么希望自己再度迷失。每一个沐浴在 爱河中的人都是诗人。 look into my eyes - you will see what you mean to me. 看看我的眼睛，你会发现你对 我而言意味着什么。distance makes the hearts grow fonder. 距离使两颗心靠得更 近。 i need him like i need the air to breathe. 我需要他，正如我需要呼吸空气。 if equal affection cannot be, let the more loving be me. 如果没有相等的爱，那就让 我爱多一些吧。 love is a vine that grows into our hearts. 爱是长在我们心里的藤蔓。
常见职位职称中英文对照
常见职位职称中英文对照 时间：2011-05-17 14:54 来源：外贸信息网 Accounting Assistant会计助理 Accounting Clerk记帐员 Accounting Manager会计部经理 Accounting Stall会计部职员 Accounting Supervisor会计主管 Administration Manager行政经理 Administration Staff行政人员 Administrative Assistant行政助理 Administrative Clerk行政办事员 Advertising Staff广告工作人员 Airlines Sales Representative航空公司定座员Airlines Staff航空公司职员 Application Engineer应用工程师 Assistant Manager副经理 Bond Analyst证券分析员 Bond Trader证券交易员 Business Controller业务主任 Business Manager业务经理 Buyer采购员 Cashier出纳员 Chemical Engineer化学工程师
Civil Engineer土木工程师 Clerk/Receptionist职员／接待员 Clerk Typist&Secretary文书打字兼秘书Computer Data Input Operator计算机资料输入员Computer Engineer计算机工程师 Computer Processing Operator计算机处理操作员Computer System Manager计算机系统部经理Copywriter广告文字撰稿人 Deputy General Manager副总经理 Economic Research Assistant经济研究助理Electrical Engineer电气工程师 Engineering Technician工程技术员 English Instructor/Teacher英语教师 Export Sales Manager外销部经理 Export Sales Staff外销部职员 Financial Controller财务主任 Financial Reporter财务报告人 F.X.(Foreign Exchange)Clerk外汇部职员 F.X.Settlement Clerk外汇部核算员 Fund Manager财务经理 General Auditor审计长 General Manager/President总经理
常用医学英文缩写对照表
常用医学英文缩写对照表 AB ACEI ACT AG AMI ANA ARDS ASO ATP AVNRT AVRT BB BEE BT BuN C3 CBC CCU CHE CK CPAP CPR CT CVP DBP DCT DIC DM EF ENT FDP FUO GNS Hb HCO3- HCT HIV Holter IABP IHSS 实际碳酸氢盐 血管紧张素转换酶抑制剂 激活凝血时间 离子间隙 急性心梗 抗核抗体 急性呼吸窘迫综合征 抗链球菌溶血素“0” 三磷酸腺苷 房室结折返性心动过速 房室折返性心动过速 缓冲碱 基础能量消耗 出血时间 尿素氮 补体C3 血常规 心血管监护室 胆碱酯酶 肌酸磷酸激酶 持续正压通气 心肺复苏 凝血时间 中心静脉压 舒张压 双氢克尿噻 弥散性血管内凝血 舒张期杂音 射血分数 耳鼻喉科(五官科) 纤维蛋白原降解产物 不明原因发热 葡萄糖生理氯化钠溶液 血红蛋白 碳酸氢根 红细胞比容 人类免疫缺陷病毒 24h动态心电图 主动脉内气囊反搏术 特发性肥厚型主动脉瓣下 NTG OB P(A-a)O2 P2 PaCO2 PAMPA PaO2 PCAP PCWP PEEP pH PPD Prn PT qh qid qn qod RF RI RR S3 S4 SaO2 SB TPN SBE SBP SGOT SGPT SK SM T3 T4 TAT TIL tid t-PA TPN TSH 硝酸甘油 隐油 肺泡气-动脉血氧分压差 肺动脉第二心音 动脉二氧化碳分压 氨甲苯酸 动脉氧分压 肺小动脉压 肺毛细血管压 呼气末正压 酸碱度 结核菌素纯蛋白衍生物 必要时 凝血酶原时间 每小时1次 每天4次 每晚1次 隔日1次 类风湿因子 胰岛素 呼吸频率 第3心音 第4心音 血氧饱和度 标准碳酸氢盐 全胃肠外营养 亚急性细菌性心内膜炎 收缩压 血清谷草转氨酶 血清谷丙转氨酶 链激酶 收缩期杂音 三碘甲状原氨酸 甲状腺素 抗蛇毒血清 短暂脑缺血发作 每天3次 组织型纤溶酶原激活物 全肠道外营养 促甲状腺激素
各种职称英文名称
文教、科技有关部门常见职衔与职称英文翻译 （大学）校长President/Chancellor （大学）副校长Vice President （大学）代理校长Acting President （中学）校长Principal （小学）校长Head /Master 学院院长Dean of College/Head of College 教务长Dean/Director of Teaching Affairs 总务长Director in Charge of General Affairs 系主任Department Chairman /Department Head 教研室主任Head of the Teaching and Research Section 实验室主任Laboratory Chief 教导主任Director of Teaching and 班主任Discipline Class Adviser/Head Teacher 教授Professor 副教授Associate Professor 客座教授Visiting Professor/Guest Professor 兼职教授Part-time Professor 名誉教授Honorary Professor 终身教授Lifetime Professor 外籍教授Foreign Professor 研究生指导教师Graduate Teacher/Research Supervisor 讲师Lecturer/Instructor
助教Teaching Assistant (T.A.) 实验员Laboratory Technician 图书馆员Librarian 研究所所长Institute Director 研究员Research Fellow/Researcher 副研究员Associate Research Fellow / Associate Researcher 助研Research Assistant 资料员Data Processor 总工程师Chief Engineer 副总工程师Assistant Chief Engineer 高级工程师Senior Engineer 工程师Engineer 助工Assistant Engineer 技术员Technician 技师Skilled Technician 董事长Chairman of the Board /Chairman 董事/理事Director 副董事Associate Director 高级会计师Senior Accountant 注册会计师(美国)Chartered Accountant 注册会计师(美国)Certified Public Accountant(CPA) 助理会计师Assistant Accountant
设计名片必备--岗位职称、部门名称中英文对照
ERP技术/应用顾问 ERP Technical/Application Consultant IC设计/应用工程师 IC Design/Application Engineer 阿拉伯语翻译 Arabic Translator 安全/健康/环境工程师 Safety/Health/Environment Engineer 安全/健康/环境经理/主管 Safety/Health/Environment Manager/Supervisor 安全人员Security Officer 办公室助理 Office Assistant 办事处财务负责人 Financial Principal in the Office 办事处代主任 Subrogating Director of the Office 办事处负责人 Principal of the Office 办事处副主任 Deputy Director of the Office 办事处客服负责人 Principal of the Customer Service in the Office 办事处主任 Director of the Office 包装设计师 Package Designer 保安 Security 保安人员 Securities Custody Clerk 保险代理/财务规划师/储备经理人 Insurance Agent/Financial Planner 保险公司理赔员 Insurance Actuary 保险核保/理赔 Adjuster 保险精算师 Actuary 保险内勤 Insurance Office Staff 报副主编 Deputy Chief Editor 报关员 Customs Specialist 本部副总经理 Assistant General Manager of the Department 本部总经理 General Manager of the Department 本部总经理高级助理 Senior Assistant of G.M. of the Department 本部总经理助理 Assistant of G.M. of the Department 本部总经理助理 Assistant of G.M. of the Department 编辑/作家/撰稿人 Editor/Writer 宾馆/酒店经理 Reception Manager 部长 Secretary 部长助理 Assistant Secretary 部门负责人 Division Principal 部门经理，科长 Section Manager 财务/会计助理 Finance/Accounting Assistant 财务/审计/统计 Finance/Accounting 财务报告人 Financial Reporter 财务分析经理/主管 Financial Analysis Manager/Supervisor 财务分析员 Financial Analyst 财务经理 Finance Manager 财务经理 Fund Manager 财务主管/总帐主管 Finance Supervisor 财务主任 Financial Controller
常见职衔与职称英文翻译
本文由雪白乌鸭贡献 文教、科技有关部门常见职衔与职称英文翻译 （大学）校长 Ｐｒｅｓｉｄｅｎｔ／Ｃｈａｎｃｅｌｌｏｒ （大学）副校长 Ｖｉｃｅ Ｐｒｅｓｉｄｅｎｔ （大学）代理校长 Ａｃｔｉｎｇ Ｐｒｅｓｉｄｅｎｔ （中学）校长 Ｐｒｉｎｃｉｐａｌ （小学）校长 Ｈｅａｄ ／Ｍａｓｔｅｒ 学院院长 Ｄｅａｎ ｏｆ Ｃｏｌｌｅｇｅ／Ｈｅａｄ ｏｆ Ｃｏｌｌｅｇｅ 教务长 Ｄｅａｎ／Ｄｉｒｅｃｔｏｒ ｏｆ Ｔｅａｃｈｉｎｇ Ａｆｆａｉｒｓ 总务长 Ｄｉｒｅｃｔｏｒ ｉｎ Ｃｈａｒｇｅ ｏｆ Ｇｅｎｅｒａｌ Ａｆｆａｉｒｓ 系主任 Ｄｅｐａｒｔｍｅｎｔ Ｃｈａｉｒｍａｎ ／Ｄｅｐａｒｔｍｅｎｔ Ｈｅａｄ 教研室主任 Ｈｅａｄ ｏｆ ｔｈｅ Ｔｅａｃｈｉｎｇ ａｎｄ Ｒｅｓｅａｒｃｈ Ｓｅｃｔｉｏｎ 实验室主任 Ｌａｂｏｒａｔｏｒｙ Ｃｈｉｅｆ 教导主任 Ｄｉｒｅｃｔｏｒ ｏｆ Ｔｅａｃｈｉｎｇ ａｎｄ 班主任 Ｄｉｓｃｉｐｌｉｎｅ Ｃｌａｓｓ Ａｄｖｉｓｅｒ／Ｈｅａｄ Ｔｅａｃｈｅｒ 教授 Ｐｒｏｆｅｓｓｏｒ 副教授 Ａｓｓｏｃｉａｔｅ Ｐｒｏｆｅｓｓｏｒ 客座教授 Ｖｉｓｉｔｉｎｇ Ｐｒｏｆｅｓｓｏｒ／Ｇｕｅｓｔ Ｐｒｏｆｅｓｓｏｒ 兼职教授 Ｐａｒｔ－ｔｉｍｅ Ｐｒｏｆｅｓｓｏｒ 名誉教授 Ｈｏｎｏｒａｒｙ Ｐｒｏｆｅｓｓｏｒ 终身教授 Ｌｉｆｅｔｉｍｅ Ｐｒｏｆｅｓｓｏｒ 外籍教授 Ｆｏｒｅｉｇｎ Ｐｒｏｆｅｓｓｏｒ 研究生指导教师 Ｇｒａｄｕａｔｅ Ｔｅａｃｈｅｒ／Ｒｅｓｅａｒｃｈ Ｓｕｐｅｒｖｉｓｏｒ 讲师 Ｌｅｃｔｕｒｅｒ／Ｉｎｓｔｒｕｃｔｏｒ 助教 Ｔｅａｃｈｉｎｇ Ａｓｓｉｓｔａｎｔ （Ｔ．Ａ．） 实验员 Ｌａｂｏｒａｔｏｒｙ Ｔｅｃｈｎｉｃｉａｎ 图书馆员 Ｌｉｂｒａｒｉａｎ 研究所所长 Ｉｎｓｔｉｔｕｔｅ Ｄｉｒｅｃｔｏｒ 研究员 Ｒｅｓｅａｒｃｈ Ｆｅｌｌｏｗ／Ｒｅｓｅａｒｃｈｅｒ 副研究员 Ａｓｓｏｃｉａｔｅ Ｒｅｓｅａｒｃｈ Ｆｅｌｌｏｗ ／ Ａｓｓｏｃｉａｔｅ Ｒｅｓｅａｒｃｈｅｒ 助研 Ｒｅｓｅａｒｃｈ Ａｓｓｉｓｔａｎｔ 资料员 Ｄａｔａ Ｐｒｏｃｅｓｓｏｒ 总工程师 Ｃｈｉｅｆ Ｅｎｇｉｎｅｅｒ 副总工程师 Ａｓｓｉｓｔａｎｔ Ｃｈｉｅｆ Ｅｎｇｉｎｅｅｒ 高级工程师 Ｓｅｎｉｏｒ Ｅｎｇｉｎｅｅｒ 工程师 Ｅｎｇｉｎｅｅｒ 助工 Ａｓｓｉｓｔａｎｔ Ｅｎｇｉｎｅｅｒ 技术员 Ｔｅｃｈｎｉｃｉａｎ 技师 Ｓｋｉｌｌｅｄ Ｔｅｃｈｎｉｃｉａｎ 董事长 Ｃｈａｉｒｍａｎ ｏｆ ｔｈｅ Ｂｏａｒｄ ／Ｃｈａｉｒｍａｎ 董事／理事 Ｄｉｒｅｃｔｏｒ 副董事 Ａｓｓｏｃｉａｔｅ Ｄｉｒｅｃｔｏｒ 高级会计师 Ｓｅｎｉｏｒ Ａｃｃｏｕｎｔａｎｔ 注册会计师（美国）Ｃｈａｒｔｅｒｅｄ Ａｃｃｏｕｎｔａｎｔ 注册会计师（美国）Ｃｅｒｔｉｆｉｅｄ Ｐｕｂｌｉｃ Ａｃｃｏｕｎｔａｎｔ（ＣＰＡ） 助理会计师 Ａｓｓｉｓｔａｎｔ Ａｃｃｏｕｎｔａｎｔ 主任会计 Ｃｈｉｅｆ Ａｃｃｏｕｎｔａｎｔ 高级经济师 Ｓｅｎｉｏｒ Ｅｃｏｎｏｍｉｃ Ｍａｎｇｅｒ ／ Ｓｅｎｉｏｒ Ｅｃｏｎｏｍｉｓｔ 经济师 Ｅｃｏｎｏｍｉｃ Ｍａｎａｇｅｒ ／Ｅｃｏｎｏｍｉｓｔ 建筑师 Ａｒｃｈｉｔｅｃｔ 规划师 Ｐｌａｎｎｅｒ
英汉互译在线翻译句子教案资料
英汉互译在线翻译句 子
美句集锦 如果只是遇见，不能停留，不如不遇见。 if we can only encounter each other rather than stay with each other,then i wish we had never encountered. 2。宁愿笑着流泪，也不哭着说后悔。心碎了，还需再补吗？ i would like weeping with the smile rather than repenting with the cry, when my heart is broken, is it needed to fix? 3。没有谁对不起谁，只有谁不懂得珍惜谁。 no one indebted for others, while many people dont know how to cherish others. 4。命里有时钟需有命里无时莫强求 you will have it if it belongs to you, whereas you dont kvetch for it if it doesnt appear in your life. 5。当香烟爱上火柴时，就注定受到伤害 when a cigarette falls in love with a match, it is destined to be hurt. 6。爱情…在指缝间承诺指缝…。在爱情下交缠。 love ,promised between the fingers finger rift, twisted in the love 7。没有人值得你流泪，值得让你这么做的人不会让你哭泣。 no man or woman is worth your tears, and the one who is, won?t make you cry. 8。记住该记住的，忘记该忘记的。改变能改变的，接受不能改变的。 remember what should be remembered, and forget what should be forgotten. alter what is changeable, and accept what is unchangeable. love is like a butterfly. it goes where it pleases and it pleases where it goes. 爱情就像一只蝴蝶，它喜欢飞到哪里，就把欢乐带到哪里。 if i had a single flower for every time i think about you, i could walk forever in my garden. 假如每次想起你我都会得到一朵鲜花，那么我将永远在花丛中徜徉。 within you i lose myself, without you i find myself wanting to be lost again. 有了你，我迷失了自我。失去你，我多么希望自己再度迷失。 每一个沐浴在爱河中的人都是诗人。 look into my eyes - you will see what you mean to me. 看看我的眼睛，你会发现你对我而言意味着什么。 distance makes the hearts grow fonder. 距离使两颗心靠得更近。 i need him like i need the air to breathe. 我需要他，正如我需要呼吸空气。 if equal affection cannot be, let the more loving be me. 如果没有相等的爱，那就让我爱多一些吧。 love is a vine that grows into our hearts. 爱是长在我们心里的藤蔓。 if i know what love is, it is because of you.
医学常用中英文名称翻译标准
常用缩写 AAA, abdominal aortic aneurysm 腹主动脉瘤 ABFB, aortobifemoral bypass 主双股动脉旁路术 ABI, ankle-brachial index 踝肱指数 ACA, anterior cerebral artery 大脑前动脉 ACE, angiotensin-converting enzyme 血管紧张素转化酶 ACT, activated clotting time 活化凝血时间 ADA, American Diabetes Association 美国糖尿病协会 ADP, adenosine diphosphate 二磷酸腺苷 AEF, aortoenteric fistula 主动脉肠道瘘 AF, atrial fibrillation 房颤 AFB, aortofemoral bypass 主股旁路术 AGE, advanced glycosylation end product 高级糖基化终末产物 AHA, American Heart Association 美国心脏病协会 AHRQ, Agency for Healthcare Research and Quality 健康保健研究及质量控制委员会AI, aortoiliac 主髂 AIDS, acquired immunodeficiency syndrome 获得性免疫缺陷综合征 AKA, above-knee amputation 膝上截肢术 AMP, adenosine monophosphate 单磷酸腺苷 APC, activated protein C 活化蛋白C APG, air plethysmography 空气体积描记术 aPTT, activated partial thromboplastin time 活化部分凝血酶原时间 ARB, angiotensin receptor blocker 血管紧张素受体阻滞剂 ARDS, acute respiratory distress syndrome 急性呼吸窘迫综合征 ARF, acute renal failure 急性肾衰 ASA, acetylsalicylic acid 阿司匹林 ATN, acute tubular necrosis 急性肾小管坏死 ATP, adenosine triphosphate 三磷酸腺苷 AVE, arteriovenous fistula 动静脉瘘 AVG, arteriovenous graft 动静脉移植物
常用名片中英文职务职称翻译大全
常用名片中英文职务职称翻译大全 千千名片多年积累整理名片中经常使用到的英文职务、职称、头衔名称的英文翻译对照，从而提高名片的翻译质量,实现跨文化交际。名片的正确英文翻译为 business card (name card ；visiting card ；calling card) ※总裁 Chief Executive ，CEO ※董事长 Board Chairman ※总经理 General Manager ※副总经理 Vice General Manager ※总经理秘书 Secretary ※总经理助理 General Manager's Assistant ※秘书 Secretary ※秘书长 secretary general ※客户经理 Account Manager ※高级理财顾问 Senior Financial Consultant ※高级客户经理 Senior Account Manager ※市场总监 Marketing Director ※客户主任 Account Executive ※市场营销部经理 Manager of Marketing Department ※销售部经理 Sales Manager ※餐饮部经理 Food and Bererage Manager ※客房部经理 Housekeeper ※Accounting Assistant 会计助理 ※Accounting Clerk 记帐员 ※Accounting Manager 会计部经理 ※Accounting Stall 会计部职员 ※Accounting Supervisor 会计主管 ※Administration Manager 行政经理 ※Administration Staff 行政人员 ※Administrative Assistant 行政助理 ※Administrative Clerk 行政办事员 ※Advertising Staff 广告工作人员 ※Airlines Sales Representative 航空公司 定座员 ※Airlines Staff 航空公司职员 ※Application Engineer 应用工程师 ※Assistant Manager 副经理 ※Bond Analyst 证券分析员 ※Bond Trader 证券交易员 ※Business Controller 业务主任 ※Business Manager 业务经理
医院各科室中英文对照
医院各科室中英文对照 急诊室——Emergency Room 医院——Hospital 内科病房——Medical Ward 外科病房——Surgical Ward 儿科病房——Pediatric Ward 接生房——Labor and Delivery 手术室——Operation Room (OR) 心脏重症室——Coronary Care Unit (CCU) 重症室——Intensive Care Unit (ICU) 内科重症室——Medical Intensive Care Unit (MICU) 初生婴儿重症室——Neonatal Intensive Care Unit (NICU) 儿科重症室——Pediatric Intensive Care Unit (PICU) 外科重症室——Surgical Intensive Care Unit (SICU) 末期护理——Hospice 居家健康服务、药疗、物理治疗等——Home Health Service 化验所（进行化验研究）——Laboratory 门诊手术中心（一般非严重性手术）——Outpatient Surgical Center 药房（药物、医疗用品）——Pharmacy 医疗服务——Health Care Provider 医生——Physician
针灸——Acupuncture 过敏性专科——Allergy and Immunology 麻醉科——Anesthesiology 心脏科——Cardiology 心胸外科——Cardio-Thoracic Surgery 脊椎神经科——Chiropractic 结肠直肠外科——Colorectal Surgery 牙科——Dentistry 皮肤科——Dermatology 内分泌科——Endocrinology 家庭科——Family Practice 肠胃科——Gastroenterology 普通全科——General Practice 普通外科——General Surgery 老人病专科——Geriatrics 血液科——Hematology 肝病专科——Hepatology 传染病科——Infectious Disease 内科——Internal Medicine 肾脏科——Nephrology 神经科——Neurology 神经外科——Neurosurgery
各种职称英文翻译
各种职称英文翻译 2007-10-16 14:33:32| 分类：职称翻译|字号大中小订阅（大学）校长Preside nt/Cha ncellor （大学）副校长Vice Preside nt （大学）代理校长Acti ng Preside nt （中学）校长Prin cipal （小学）校长Head /Master 学院院长Dean of College/Head of College 教务长Dean/Director of Teaching Affairs 总务长Director in Charge of General Affairs 系主任Department Chairman /Department Head 教研室主任Head of the T eaching and Research Section 实验室主任Laboratory Chief 教导主任Director of Teach ing and 班主任Discipline Class Adviser/Head Teacher 教授Professor 副教授Associate Professor 客座教授Visiting Professor/Guest Professor 兼职教授Part-time Professor
叮叮小文库名誉教授Honorary Professor 终身教授Lifetime Professor 外籍教授Foreig n Professor 研究生指导教师Graduate Teacher/Research Supervisor 讲师Lecturer/Instructor 助教Teachi ng Assista nt (T.A.) 实验员Laboratory Tech nician 图书馆员Libraria n 研究所所长In stitute Director 研究员Research Fellow/Researcher 副研究员Associate Research Fellow / Associate Researcher 助研Research Assistant 资料员Data Processor 总工程师Chief Engineer 副总工程师Assista nt Chief Engin eer 高级工程师Se nior En gi neer 工程师Engineer 助工Assistant Engineer 技术员Technician
常用职称职位英文翻译
常用职称职位英文翻译 董事长Board Chairman 总经理General Manager 副总经理Vice General Manager 总经理秘书Secretary 总经理助理General Manager's Assistant 市场营销部经理Manager of Marketing Department 销售部经理Sales Manager 餐饮部经理Food and Bererage Manager 客房部经理Housekeeper 康乐部经理Recreation Dept Manager 财务部经理Financial Controller 人事部经理Personnel Manager 工程部经理Chief Engineer 保安部经理Chief Security Officer 办公室主任Director of Executive Office 大堂副理Asst Manager 物资经理Logistic & Purchasing Dept.Manager 会计Accountant 销售工程师Sales Engineer 生产经理Production Dept.Manager 销售工程师Sales Engineer 工会主席Labour Union chairman 操作工Operator 库管员Warehouse Keeper 技术工程师Technicial Engineer 销售一部经理Sales Dept.Manager 接待员Receiptionalist 配料员Operator 保洁员Purifier 人事经理助理HR Assistant 炊事员Canteen Worker 会计Accountant 质保经理QC Dept.Manager 机械师Machinist 工程主管Facilities Supervisor 采购员Buyer 车间班长Group Leader 叉车司机Driver 机修工Operator 采购主管Purchase Manage
常用临床医学英文缩写中英文对照
常用临床医学英文缩写中英文对照 AB 实际碳酸氢盐红细胞计数 RBC AB实际碳酸氢盐 ACEI 血管紧张素转换酶抑制 白细胞计数 WBC ACEI血管紧张素转换酶抑制剂剂 ACT 激活凝血时间血小板计数 BPC ACT激活凝血时间AG 离子间隙血红蛋白 Hb AG离子间隙 AMI 急性心梗网织红细胞计数 Ret.C AMI急性心梗 ANA 抗核抗体白细胞分类计数 WBC DC ANA抗核抗体 ARDS 急性呼吸窘迫综合征红细胞沉降率 ESR ARDS急性呼吸窘迫综合征ASO 抗链球菌溶血素“0” 尿素氮 BUN ASO抗链球菌溶血素“0” ATP 三磷酸腺苷肌酐 Cr ATP三磷酸腺苷AVNRT 房室结折返性心动过速淀粉酶 AMS AVNRT房室结折返性心动过速AVRT 房室折返性心动过速甲状腺素 T4AVRT房室折返性心动过速BB 缓冲碱三碘甲腺原氨酸 T3BB缓冲碱 血糖 & 空腹血糖 BG & BEE 基础能量消耗 BEE基础能量消耗 FBG BT 出血时间红斑狼疮细胞 LEC BT出血时间 BuN 尿素氮免疫球蛋白G lgG BuN尿素氮 C3 补体C3 免疫球蛋白A lgA C3补体C3 CBC 血常规免疫球蛋白M lgM CBC血常规CCU 心血管监护室免疫球蛋白D lgD CCU心血管监护室CHE 胆碱酯酶免疫球蛋白E lgE CHE胆碱酯酶 CK 肌酸磷酸激酶CK肌酸磷酸激酶 CPAP 持续正压通气CPAP持续正压通气CPR 心肺复苏CPR心肺复苏 CT 凝血时间CT凝血时间
CVP 中心静脉压CVP中心静脉压DBP 舒张压DBP舒张压DCT 双氢克尿噻DCT双氢克尿噻DIC 弥散性血管内凝血DIC弥散性血管内凝血DM 舒张期杂音DM舒张期杂音 EF 射血分数EF射血分数ENT 耳鼻喉科(五官科) ENT耳鼻喉科(五官科) FDP 纤维蛋白原降解产物FDP纤维蛋白原降解产物FUO 不明原因发热FUO不明原因发热GNS 葡萄糖生理氯化钠溶液GNS葡萄糖生理氯化钠溶液Hb 血红蛋白Hb血红蛋白HCO3- 碳酸氢根HCO3-碳酸氢根 HCT 红细胞比容HCT红细胞比容HIV 人类免疫缺陷病毒HIV人类免疫缺陷病毒Holter 24h动态心电图Holter24h动态心电图IABP 主动脉内气囊反搏术IABP主动脉内气囊反搏术IHSS 特发性肥厚型主动脉瓣下 狭窄IHSS 特发性肥厚型主动脉瓣下狭 窄 INR 国际标准比率INR国际标准比率IU 国际单位IU国际单位KPTT 部分凝血活酶时间KPTT部分凝血活酶时间KUB 腹部平片KUB腹部平片LDH 乳酸脱氢酶LDH乳酸脱氢酶NS 生理氯化钠溶液NS生理氯化钠溶液NTG 硝酸甘油NTG硝酸甘油OB 隐油OB隐油
名片常用的100个职称、职务、头衔名称的英文翻译
董事长Board Chairman总经理General Manager副总经理Vice General Manager执行副总经理Executive Vice President执行副总Deputy General总经理秘书Secretary总经理助理General Manager's Assistant市场营销部经理Manager of Marketing Department销售部经理Sales Manager餐饮部经理Food and Bererage Manager客房部经理Housekeeper康乐部经理Recreation Dept Manager财务部经理Financial Controller人事部经理Personnel Manager工程部经理Chief Engineer保安部经理Chief Security Officer办公室主任Director of Executive Office大堂副理Asst Manager物资经理Logistic&；Purchasing Dept.Manager会计Accountant销售工程师Sales Engineer生产经理Production Dept.Manager销售工程师Sales Engineer工会主席Labour Union chairman操作工Operator 库管员Warehouse Keeper技术工程师Technicial Engineer销售一部经理Sales Dept.Manager接待员Receiptionalist配料员Operator保洁员Purifier人事经理助理HR Assistant炊事员Canteen Worker会计Accountant质保经理QC Dept.Manager机械师Machinist工程主管Facilities Supervisor采购员Buyer车间班长Group Leader叉车司机Driver机修工Operator采购主管Purchase Manage综合管理部Colligation and Management Dep财务部部长Finance Dep.Minister市场部部长助理Market Dep.Ministe r's assistant 生产部部长助理Produce Dep.Ministarls assistant研发工程师Develop Engineer业务主办Operation Direct计划员Programmer更夫Bellman技术服务部经理Technical Service Dept.Manager物资内勤Secretary技术服务工程师Technician Service Engineer销售二部经理Sales Dept.Manager车间主管Production Supervisor内勤Secretary出纳Cashier 检验员hecker市场部经理Marketing Dept.Manager区域销售经理Regional Sales Manager IT工程师IT Engineer研磨工Operator司机Driver清扫工Purifier人力资源部经理Human Resources Manager文员Clerk财务经理Finance Dept.Manager技术发展部经理Technical Development Dept.Manager电工Electrician送货员Deliveryman挤压工Operator