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Describes the use of the Agilent 8890 GC to analyze impurities in sartan products according to a United States Food and Drug Administration (US FDA) method.
| Chinese (Simplified) (China) | Complete (PDF) |
|---|---|
| Italian (Italy) | Complete (PDF) |
| Portuguese (Brazil) | Complete (PDF) |
| Korean (Korea) | Complete (PDF) |
| French (France) | Complete (PDF) |
| Spanish (Spain) | Complete (PDF) |
| German (Germany) | Complete (PDF) |
A GC/FID/MSD method for the residual solvents.
使用 Agilent 8890 氣相色譜系統(tǒng)和所選色譜柱通過(guò) USP 方法 對(duì)殘留溶劑進(jìn)行分析的方法
| Korean (Korea) | Complete (PDF) |
|---|---|
| Italian (Italy) | Complete (PDF) |
| French (France) | Complete (PDF) |
| Portuguese (Brazil) | Complete (PDF) |
| German (Germany) | Complete (PDF) |
| Spanish (Spain) | Complete (PDF) |