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The Agilent workflow solution for implementing an elemental impurities analysis capability in compliance with USP / and ICH Q3D.
| English (United States) | Complete (PDF) |
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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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New limits for elemental impurities in pharmaceutical materials and dietary supplements have been released by the USP and ICH.
Expanded support for USP / and ICH Q3D methods supports compliance with elemental impurity analysis in pharmaceutical materials via ICP-OES
White paper discussing the important considerations for implementing an elemental impurities analysis capability in compliance with USP / and ICH Q3D.