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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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Study using USP method quantified 24 elements via ICP-MS in pharmaceutical materials dissolved in organic solvent (DMSO)
SDA Compliance for Agilent ICP-MS Systems
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.
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...