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應用的篩選條件
This application note demonstrates the use of the handheld Vaya Raman system, for the identification of mRNA LNPs through transparent and opaque containers.
New limits for elemental impurities in pharmaceutical materials and dietary supplements have been released by the USP and ICH.
Learn about proven workflows for regulatory compliance, enhance drug quality and safety, simplify analysis with cutting-edge technology.
Compares Analytical Instrument Qualification using Agilent ACE with other options using Data Integrity and compliance with USP general chapter as a framework.
The Agilent workflow solution for implementing an elemental impurities analysis capability in compliance with USP / and ICH Q3D.
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
Expanded support for USP / and ICH Q3D methods supports compliance with elemental impurity analysis in pharmaceutical materials via ICP-OES
This application note demonstrates the benefits of combining helium collision mode and discrete sampling to develop and validate an easy-to-use, polyatomic interference-free method for the determination of 13 elements in tea infusion.
| 文件出版號 | 5991-3252EN | |||
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| 分析 | 分析采用的部件號. |
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| 分析技術 | 技術 |
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| 樣品 | 化學基團 |
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Agilent 8697 ヘッドスペースサンプラ（HSS）と水素炎イオン化検出器（FID）を搭載した 8890 ガスクロマトグラフ（GC）を用いて、窒素および水素キャリアガスにより日本薬局方殘留溶媒試験のクラス 1、2A、2B の溶媒を測定しました。水溶性試料および非水溶性試料について適合性を満たし...
Agilent 8697 ヘッドスペースサンプラ（HSS）と水素炎イオン化検出器（FID）を搭載した 8890 ガスクロマトグラフ（GC）を用いてヘリウムキャリアガスにより日本薬局方殘留溶媒試験のクラス 1、2A、2B の溶媒を測定しました。水溶性試料および非水溶性試料について適合性を満たしました。...