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Impurities in Isavuconazole are identified using analytical techniques such as chromatography, spectroscopy, and mass spectrometry. Comparison with reference standards or known impurities aids in identification.
Impurities in Isavuconazole are tested and monitored throughout the synthesis. Regular testing ensures compliance with regulatory guidelines and maintains the quality of the medication.
Quantification of impurities in Isavuconazole uses validated analytical methods. Calibration curves are generated using known reference standards to determine their concentration.
The recommendation is to store Isavuconazole impurities at a controlled room temperature, within 2-8 °C.
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