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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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SDA Compliance for Agilent ICP-MS Systems
White paper discussing how Agilent’s MassHunter & OpenLAB Server software supports compliance to GLP & GMP regulations.
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.