MIL-D-85520
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来源:标准资料网
MIL-D-85520, MILITARY SPECIFICATION: DESIGN AND INSTALLATION OF ON BOARD OXYGEN GENERATING SYSTEMS IN AIRCRAFT, GENERAL SPECIFICATION FOR (10 MAR 1983)., This specification covers the general requirements for the design and installation of on board oxygen generating systems (OBOGS) in military aircraft
【英文标准名称】:BroadbandIntegratedServicesDigitalNetwork(B-ISDN)-DigitalSubscriberSignallingSystemNo.two(DSS2)protocol;Connectioncharacteristics;Negotiationduringcall/connectionestablishmentphase-Part6:AbstractTestSuite(ATS)andpartialProto
【原文标准名称】:宽带综合业务数字网(B-ISDN).数字用户信令系统No.2(DSS2)协议.连接特性.呼叫/连接建立阶段协商.第6部分:网络用抽象试验成套试验装置(ATS)和部分实施试验协议附加信息格式规范(PIXIT)
【标准号】:DINEN301067-6-2001
【标准状态】:现行
【国别】:德国
【发布日期】:2001-09
【实施或试行日期】:
【发布单位】:德国标准化学会(DIN)
【起草单位】:
【标准类型】:()
【标准水平】:()
【中文主题词】:用户系统;无线电装置;传播技术;呼叫;信息处理;规范;远程通信;附加信息;综合服务数字网络;试验要求;信号发送系统;宽带综合业务数字网;无线电电路;综合业务数字网;电路网络;宽带网络;通信;协议;电信;电信;连接线;连接
【英文主题词】:
【摘要】:Thedocumentspecifiesrequirementsinthetelecommunicationsector.
【中国标准分类号】:M11
【国际标准分类号】:33_080
【页数】:1P;A4
【正文语种】:德语
【英文标准名称】:Clinicalinvestigationofmedicaldevicesforhumansubjects-Part1:Generalrequirements(ISO14155-1:2003);GermanversionENISO14155-1:2003
【原文标准名称】:医学受验者用医疗设备的临床调查.第1部分:一般要求
【标准号】:DINENISO14155-1-2003
【标准状态】:作废
【国别】:德国
【发布日期】:2003-09
【实施或试行日期】:
【发布单位】:德国标准化学会(DE-DIN)
【起草单位】:
【标准类型】:()
【标准水平】:()
【中文主题词】:人;牙科器械;结果;利用;牙科设备;文献工作;检验师;临床医学;临床调查;性能试验;医疗设备;试验;规范(验收);医疗产品;外科植入物;外科植入物;医疗技术学;手术器械;评定;定义;安全;效率;企业;临床试验;人体;医学科学;监督(认可);报告
【英文主题词】:Clinicalinvestigations;Clinicalmedicine;Clinicaltesting;Controlcharts;Definitions;Dentalequipment;Dentalinstruments;Documentations;Efficiency;Enterprises;Evaluations;Humanbody;Implants(surgical);Information;Inspectors;Medicaldevices;Medicalequipment;Medicalproducts;Medicalsciences;Medicaltechnology;People;Performancetesting;Reports;Results;Safety;Specification(approval);Surgicalimplants;Surgicalinstruments;Surveillance(approval);Systemology;Testpersons;Testing;Trials;Utilization
【摘要】:ThisInternationalStandarddefinesproceduresfortheconductandperformanceofclinicalinvestigationsofmedicaldevices.Itspecifiesgeneralrequirementsintendedtoprotecthumansubjects;ensurethescientificconductoftheclinicalinvestigation;assistsponsors,monitors,investigators,ethicscommittees,regulatoryauthoritiesandbodiesinvolvedintheconformityassessmentofmedicaldevices.ThisInternationalStandardpertainstoallclinicalinvestigation(s)ofmedicaldeviceswhoseclinicalperformanceandsafetyisbeingassessedinhumansubjects;specifiesrequirementsfortheconductofaclinicalinvestigationsuchthatitdemonstratesthatthemedicaldeviceachievestheperformanceintendedbythemanufacturer,revealsanyadverseeventsundernormalconditionsofuseandpermitassessmentoftheacceptableriskshavingregardtotheintendedperformanceofthemedicaldeviceandspecifiesrequirementsfortheorganization,designincludingmethodology,conduct,monitoring,datacollection,documentationandevaluationofresultsoftheclinicalinvestigationofamedicaldevice.ThisInternationalStandarddoesnotapplytoin-vitrodiagnosticmedicaldevices.
【中国标准分类号】:C30
【国际标准分类号】:11_100_20
【页数】:30P.;A4
【正文语种】:德语
