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Agilent Atomic Absorption Spectrometers deliver high performance that analysts require while being equally at home in routine labs where reliabiltiy is vital.
The Agilent workflow solution for implementing an elemental impurities analysis capability in compliance with USP / and ICH Q3D.
| English (United States) | Complete (PDF) |
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This application note describes the validation of a procedure for the measurement of elemental impurities in sterile artificial tear eye drops (SATED).
Reducing the time and expense of ICP-MS method development and system validation for measuring elemental impurities in pharmaceuticals
Study using USP method quantified 24 elements via ICP-MS in pharmaceutical materials dissolved in organic solvent (DMSO)
The analysis of 24 elements in Aspirin samples using an Agilent ICP-OES and the analytical procedures and validation studies required by USP / ICH-Q3D.
| Chinese (Simplified) (China) | Complete (PDF) |
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Metallic impurities in trichlorosilane (TCS), an intermediate product used in the production of photovoltaic (PV) silicon, must be strictly controlled in order to produce...
| Chinese (Simplified) (China) | Complete (PDF) |
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Application note for Simple, Reliable Analysis of High Matrix Samples According to US EPA Method 6020A using the Agilent 7700x/7800 ICP-MS
The Agilent 7900 ICP-MS with UHMI and ISIS discrete sampling was able to analyze both trace levels and higher concentrations of elements in acid digested geological samples.
| Korean (Korea) | Complete (PDF) |
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SDA Compliance for Agilent ICP-MS Systems
ICP-MS method for measuring both major and trace elements in food samples in a single analytical run.
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Deliver accurate and reproducible results for the analysis of major and trace elements in domestic sludge with reduced operating costs compared to FAAS.
Application note for the determination of K, Na, and Zn in Albumin using Flame AAS
Application note for new high performance graphite furnace tube for determination of lead in blood
White paper discussing how Agilent’s MassHunter & OpenLAB Server software supports compliance to GLP & GMP regulations.
New limits for elemental impurities in pharmaceutical materials and dietary supplements have been released by the USP and ICH.
Expanded support for USP / and ICH Q3D methods supports compliance with elemental impurity analysis in pharmaceutical materials via ICP-OES
White paper discussing the important considerations for implementing an elemental impurities analysis capability in compliance with USP / and ICH Q3D.
White paper discussing the important considerations for implementing an elemental impurities analysis capability in compliance with USP / and ICH Q3D.
ICH and USP tests for elemental impurities provide better indication of potentially toxic contaminants. Learn more...