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The Agilent workflow solution for implementing an elemental impurities analysis capability in compliance with USP / and ICH Q3D.
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Reducing the time and expense of ICP-MS method development and system validation for measuring elemental impurities in pharmaceuticals
Application note for Simple, Reliable Analysis of High Matrix Samples According to US EPA Method 6020A using the Agilent 7700x/7800 ICP-MS
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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New limits for elemental impurities in pharmaceutical materials and dietary supplements have been released by the USP and ICH.
White paper discussing the important considerations for implementing an elemental impurities analysis capability in compliance with USP / and ICH Q3D.