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White paper discussing how Agilent’s MassHunter & OpenLAB Server software supports compliance to GLP & GMP regulations.
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)
White paper discussing the important considerations for implementing an elemental impurities analysis capability in compliance with USP / and ICH Q3D.
Compound structure-independent quantificatio of drugs
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.
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.
White paper discussing the important considerations for implementing an elemental impurities analysis capability in compliance with USP / and ICH Q3D....