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了解根據(jù) USP 章節(jié) 要求將方法轉(zhuǎn)移至 UHPLC 條件如何能夠節(jié)省溶劑和分析時(shí)間。
- 文件出版號(hào): 5994-6126ZHCN
- 創(chuàng)建日期: 28 七月 2023
- 641 KB
White paper discussing how Agilent’s MassHunter & OpenLAB Server software supports compliance to GLP & GMP regulations.
- 文件出版號(hào): 5991-2593EN
- 創(chuàng)建日期: 10 十月 2024
- 876 KB
White paper discussing how Agilent’s ICP-MS MassHunter and OpenLab ECM software supports compliance to Part 11 & Annex 11 regulations
- 文件出版號(hào): 5991-1925EN
- 創(chuàng)建日期: 01 十月 2024
- 1 MB
LC/MS based characterization workflow of the GLP-1 therapeutic peptide liraglutide and its impurities using the 1290 Infinity II LC and 6545XT AdvanceBio LC/Q-TOF.
- 文件出版號(hào): 5994-7727EN
- 創(chuàng)建日期: 25 九月 2024
- 3 MB
This application note describes the validation of a procedure for the measurement of elemental impurities in sterile artificial tear eye drops (SATED).
- 文件出版號(hào): 5994-1561EN
- 創(chuàng)建日期: 16 十月 2023
- 1 MB
Reducing the time and expense of ICP-MS method development and system validation for measuring elemental impurities in pharmaceuticals
- 文件出版號(hào): 5991-8335EN
- 創(chuàng)建日期: 16 十月 2023
- 995 KB