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使用 Agilent 5110 SVDV ICP-OES 對阿司匹林樣品中 24 種目標(biāo)元素的分析和 USP /ICH-Q3D 規(guī)定的分析流程和驗(yàn)證研究。
| 英語 (美國) | 完整版（PDF） |
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New limits for elemental impurities in pharmaceutical materials and dietary supplements have been released by the USP and ICH.
The Agilent workflow solution for implementing an elemental impurities analysis capability in compliance with USP / and ICH Q3D.
| 英語 (美國) | 完整版（PDF） |
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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.