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Reducing the time and expense of ICP-MS method development and system validation for measuring elemental impurities in pharmaceuticals
- Publication Part Number: 5991-8335EN
- Created: 16 Oct 2023
- 995 KB
Study using USP method quantified 24 elements via ICP-MS in pharmaceutical materials dissolved in organic solvent (DMSO)
- Publication Part Number: 5991-7674EN
- Created: 29 Oct 2021
- 890 KB
Compound structure-independent quantificatio of drugs
- Publication Part Number: 5991-9077EN
- Created: 22 Mar 2018
- 485 KB
White paper discussing the important considerations for implementing an elemental impurities analysis capability in compliance with USP / and ICH Q3D.
- Created: 11 Aug 2021
- 3 MB
必威体育登录手机White paper discussing how Agilent's MassHunter & OpenLAB Server software supports compliance to GLP & GMP regulations.
- Publication Part Number: 5991-2593EN
- Created: 02 Mar 2021
- 907 KB
White paper discussing the important considerations for implementing an elemental impurities analysis capability in compliance with USP / and ICH Q3D.
- Created: 10 Jan 2018
- 304 KB
White paper discussing the important considerations for implementing an elemental impurities analysis capability in compliance with USP / and ICH Q3D....
- Publication Part Number: 5991-8149JAJP
- Created: 26 May 2017
- 887 KB
White paper discussing the important considerations for implementing an elemental impurities analysis capability in compliance with USP / and ICH Q3D.
- Created: 26 May 2017
- 329 KB
White paper discussing the important considerations for implementing an elemental impurities analysis capability in compliance with USP / and ICH Q3D.
- Created: 26 May 2017
- 338 KB
White paper discussing the important considerations for implementing an elemental impurities analysis capability in compliance with USP / and ICH Q3D.
- Created: 26 May 2017
- 311 KB