Shimadzu Corp.
It is a leading global producer of analytical instruments, laboratory equipment, medical diagnostic systems (such as X-ray and imaging systems), and industrial machinery.
- 81-75-823-1111
- 1 Nishinokyo Kuwabara-cho
Nakagyo-ku
Kyoto, 604-8511
Japan
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Product
LC/MS/MS Method Package For Lipid Mediators
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Lipid mediators (bioactive lipids) have important physiological functions and have been associated with allergies, thrombosis and lifestyle-related diseases. This method package provides a simultaneous analysis method that encompasses totally 214 compounds, which include 196 compounds of lipid mediators derived from arachidonic acid cascade and 18 internal standard compounds.
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Product
On-line Water Quality Analysis
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Shimadzu is one of the world’s leading manufacturers of high-quality continuous monitoring systems that meet the application requirements of a wide range of customers for environmental testing, pharmaceuticals, chemicals, and academic research, etc.
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Product
Electromagnetic Force Micro Tester
Micro-Servo
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This is a multi-functional fatigue testing machine suitable for specimens, structures and full-sized parts. It is an overhead actuator type with a broad test space, so it is ideal for various types of environmental tests, such as those in corrosion tanks or constant temperature tanks.
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Product
Axial Force And Torsion Testing Machine
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Evaluation Testing That Approximates Operating Conditions of Materials and Parts - Loading methods similar to actual usage - Allows simultaneous application of axial and torsional loads to samples
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Product
VUV PIONA+ Analysis
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This high-speed gasoline PIONA analyzer is compliant with ASTM D8071. It supports simultaneous analysis of PIONA compounds, specific oxygenated compounds, and BTEX in gasoline, and can quickly analyze samples within 30 minutes by classifying compounds based on VUV absorption spectra. The simple system configuration provides broad applicability, including analyzing other petroleum products.
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Product
AXIMA Performance - A Highly Flexible Research-grade Mass Spectrometer
AXIMA Performance
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The AXIMA Performance is one of the most powerful tools in mass spectrometry, delivering information-rich spectra with greater sensitivity and higher confidence in identification. It is an extremely versatile and powerful TOF-TOF system, integrating workflows for a diverse range of analytical needs.
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Product
Servopulser Fatigue And Endurance Testing Machine
EHF-E Series
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This is the standard electrohydraulic servo fatigue testing machine, offering outstanding stable performance. It is capable of carrying out tests ranging from static tests to fatigue tests.
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Product
LC/MS/MS Method Package For Primary Metabolites
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Shimadzu Method Packages deliver conditions for efficient and simultaneous multi-component analysis. They enable the user to quickly and easily implement complex methods without costly and laborious method development by providing sample preparation protocols, LC separation conditions, and MS acquisition parameters.
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Product
Energy Dispersive X-ray Fluorescence Spectrometer
Pharmaceutical Elemental Impurities Analysis System
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Control of Elemental Impurities in Pharmaceuticals In the pharmaceutical industry, the analysis of elemental impurities is necessary to ensure the safety of pharmaceuticals. In December 2014, the "Guideline for Elemental Impurities" (Q3D) was issued by the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH), consisting of representatives from Europe, the U.S. and Japan. In Japan, the "Guideline for Elemental Impurities in Drug Products" (PFSB/ELD Notification 0930 #4 from the Ministry of Health, Labour and Welfare) was issued, and will be applied to new drug products submitted for approval after April 1 2017. For 24 elements categorized in Class 1 to Class 3, residual quantities in pharmaceutical drug products must be controlled within permissible limits. Although ICP-AES and ICP-MS are used for precise analysis of elemental impurities, X-ray fluorescence spectrometers can be used as an alternative analysis method. This is because they can quantitatively and qualitatively analyze a variety of elements nondestructively, and without chemical pretreatment, unlike ICP-AES and ICP-MS systems. The X-ray fluorescence spectrometry has been adopted as a general method of analysis in the U.S Pharmacopeia and the European Pharmacopoeia. (USP<735>, Ph.Eur.2.2.37)
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Product
HPLC/UHPLC/SFC Systems
Nexera series
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Shimadzu has long been advancing the analytical performance of HPLC systems. At the same time, we recognize that overall efficiency depends not only on the performance of one instrument, but on the management of all devices within a lab. This realization leads us to now, a time in which AI capabilities have been incorporated to allow devices to detect and resolve issues automatically. In addition, lab management has been integrated using the Internet of Things (IoT) and device networking, making it simple to review the status of instruments and optimize resource allocation.
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Product
Application Specific LC Systems
Co-Sense for Impurities
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The FDA draft guidance, "Genotoxic and Carcinogenic Impurities in Drug Substances and Products: Recommended Approaches" prescribes permitted limits for genotoxic impurities in drug substances. These impurities demand more sensitive trace-level analysis than normal impurities. Generally, mass spectrometry methods, such as GC/MS or LC/MS, are used for the high-sensitivity analysis of impurities. However, there is increasing demand for the establishment of a high-sensitivity quantitation method using an absorbance or other conventional detector that is easy to operate and can easily apply existing LC analysis conditions.
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Product
LC/MS/MS Method Package For Water Quality Analysis
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Shimadzu provides method files, including pre-registered MRM parameters with optimized quantitative and reference ions, LC separation parameters, and retention times and peak identification parameters for each compound, as well as report templates for outputting quantitation results, as a package. If retention times are adjusted when the system is introduced, based on the HPLC configuration delivered, the analysis process can be started as soon as the specified columns, mobile phases, and standard samples are supplied.
















