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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.
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
The Agilent workflow solution for implementing an elemental impurities analysis capability in compliance with USP / and ICH Q3D.