VALIDATION OF UV-SPECTROMETRY ASSAY METHOD FOR DISSOLUTION PROFILE TEST FOR MOXIFLOXACINE TABLETS
Validation of UV-spectrometry assay method for dissolution profile test for levofloxacine tablets was carried out. The evaluated validation characteristics were: specificity, linearity, accuracy, precision, and analytical range. It was shown than main validation characteristics meet the Russian Stat...
| Päätekijät: | , , , , , |
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| Aineistotyyppi: | Artikkeli |
| Kieli: | Russian |
| Julkaistu: |
LLC Center of Pharmaceutical Analytics (LLC «CPHA»)
2019-01-01
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| Sarja: | Разработка и регистрация лекарственных средств |
| Aiheet: | |
| Linkit: | https://www.pharmjournal.ru/jour/article/view/89 |