共查询到18条相似文献,搜索用时 109 毫秒
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根据资质认定、实验室认可要求,从仪器设备管理的要求和仪器设备管理工作实际出发,归纳了实验室仪器设备管理、计量溯源方面的要求以及管理环节中容易出现的问题,采用用户界面(user interface,UI)插件技术和Gojs技术开发了信息管理系统仪器设备管理模块,降低了系统维护的难度,满足了系统使用的个性化需求,实现了仪器... 相似文献
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食品检测实验室大型检测设备的管理探讨 总被引:1,自引:0,他引:1
从食品实验室大型设备定义、仪器设备购置、使用管理、人员管理、共享管理、网络化管理、设备报废7个方面对食品检测实验室大型检测设备的管理进行了探讨,尤其是对量值传递/溯源、仪器使用人员管理提出了建议. 相似文献
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针对扫描电子显微镜(SEM)实验室数据传输的问题,将局域网运用到SEM实验室中,对实验室现有设备进行局域网的组建,组建的局域网具有方便、快捷、提高工作效率且便于规范统一管理流程的优点.提出的方案可以应用于其它分析实验室多台仪器设备数据的传输. 相似文献
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《理化检验(化学分册)》2016,(2)
正1实验室信息管理系统(LIMS)1.1什么是LIMS LIMS能够完成实验室数据和信息的收集、分析、报告和管理。LIMS基于计算机局域网,专门针对一个实验室的整体环境而设计,是一个包括了信号采集设备、数据通讯软件、数据库管理软件的高效集成系统[1]。LIMS以实验室为中心,将实验室的业务流程、环境、人员、仪器设备、标准物质、标准溶液、化学试剂、标准方法、图书资料、文件记录、科研 相似文献
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韩玉刚 《分析测试技术与仪器》2020,26(2):87-89
正中国科学院生物物理研究所是国家生命科学领域基础研究机构.研究所拥有生物大分子和脑与认知科学两个国家重点实验室、感染与免疫和核酸生物学两个中国科学院重点实验室.蛋白质科学研究平台是研究所公共技术服务中心,负责研究所50万元以上设备开放共享运行管理,为研究所和所外用户提供高水平的技术支撑服务.生物物理研究所长期致力于生命科学关键仪器设备创新研制,高度重视大型仪器设备开放共享,高度重视技术支撑系统的建设,积累了一系列可复制、可推广的成功经验. 相似文献
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PDS(Photomaric Data Acquisition System)的主要技术指标指的是该仪器的一些性能指标的极限值。由于在实际工作中,光密度精度和坐标精度与仪器的线性、噪声、速度、扫描方向、步长、孔径等参数相互依赖和制约,所以必须弄清它们之间的关系,才能够获得高精度的数据。然而每台PDS显微密度计之间,这些相互制约的性能有很大的离散性,因此使某些参数的选取无固定方式,必须因不同型号的仪器和被研究图象的特征而变。为此,我们对本室引进的精密仪器PDS显微密度计的主要性能进行了测试及分析,获得了较为满意的测试及分析结果,可供PDS用户操作人员参考。 相似文献
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李晓敏 《分析测试技术与仪器》2021,27(1):36-43
带冷冻传输系统的双束扫描电镜可实现样品原生态下的高分辨图像采集,以及冷冻含水样品的超薄切片制备,而被广泛应用于生命、医学、食品、化学、材料等领域,在相关科学研究中逐渐体现出不可取代的地位. 介绍了带冷冻系统扫描电镜的基本配置,并重点从开放共享与成效、仪器常见故障及维护等方面详细阐述了仪器的科学管理,以提高仪器的使用效率,为同类型仪器的运行提供管理经验. 相似文献
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L. Huber 《Accreditation and quality assurance》1999,4(3):87-89
To help users of laboratory instrumentation to obtain laboratory accreditation and International Organization of Standardization
certification, instrument manufactures should develop a comprehensive compliance programme for their products that includes
product features, documentation and services for equipment validation and qualification.
Received: 5 October 1998 · Accepted: 20 October 1998 相似文献
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Analytical laboratories are more and more faced to meet official regulatory requirements as described in FDA and EPA good laboratory practice, good automated laboratory practice and good manufacturing practice regulations or to officially establish quality systems, such as specified in the ISO 9000 Series quality standards, in the ISO Guide 25 or in the EN 45001 guidelines. The impact on analytical instrumentation will be the requirement for stringent validation of analytical equipment and methods which increase the overall analysis costs. An overview is presented on the validation requirements using e.g. gas chromatography, high performance liquid chromatography, capillary electrophoresis and UV-visible spectroscopy and on the strategy to meet such needs at minimal extra costs with the help of an instrument vendor. It is recommended to use instrument hardware that has already built-in tools for self-verification and which is to be validated at the vendor's site. Performance testing in the user's laboratory is done using standard operating procedures as supplied with the instrument. If resources in the user's laboratory are limited, the performance verification is done by the vendor. Software and the entire computer system is validated prior to shipment at the vendor's site. Acceptance testing is done in the user's environment following the vendor recommendations. Analytical methods are validated automatically at the end of method development using a dedicated software. The software can be customized such that it can also be used for daily automated system suitability testing. Security and integrity of analytical data are ensured by saving the raw data together with instrument conditions and instrument log-books in check-sum protected binary register files for long-term archiving. 相似文献
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L. Huber 《Accreditation and quality assurance》1996,1(1):24-34
The quality process for commercial analytical equipment starts with the selection of the vendor. It is recommended that vendors
be selected who are recognized as having quality processes in place for instrument design, development, manufacturing, testing,
service, and support, for example, ISO 9001 registration. When the instrument arrives in the laboratory, the installation
process should follow well-documented procedures. This includes a visual inspection that the instrument is not damaged and
checking that the instrument, documentation and accessories such as cables and tubings are complete. Before the instrument
is used it should be verified that it meets functional and performance specification. During operation the instruments should
be periodically inspected and tested, verified to meet performance, and calibrated. The instrument should be labeled with
the calibration status, indicating the dates of the last successful and the next performance verification and calibration.
Defective instruments should be removed from the testing area or should at least be labeled as being "out of order."
Received 23 August 1995 Accepted 6 September 1995 相似文献
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计算机在化学实验室自动化管理方面的应用 总被引:2,自引:0,他引:2
介绍了计算机技术在化学实验室自动化管理方面的应用动态,包括国内外在实验室信息自动化管理系统(LIMS)、实验室化学药品与材料管理系统(MIS)和实验室设备维护与校正管理系统(IMCS)的最新进展,以及上述计算机系统在实验室自动化管理方面的特点和作用。 相似文献
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M Mayer R Heikkinen T Omtoft 《Journal of the International Federation of Clinical Chemistry》1996,8(1):20-21
Laboratory cost management deals with the economical use of laboratory resources such as capital, equipment and manpower. Cost analysis is a tool for cost management, by means of which the laboratory manager can properly set priorities, choose appropriate test procedures, set personnel policies and make better investments of his resources. This article sets out some important aspects of cost analysis, such as the construction of cost curves, the factors that enter into cost analysis, the context in which cost analysis is used, and the limitations of this type of analysis. 相似文献