Разработка и регистрация лекарственных средств (Jan 2019)

VALIDATION OF UV-SPECTROMETRY ASSAY METHOD FOR DISSOLUTION PROFILE TEST FOR LEVOFLOXACINE TABLETS

  • A. A. Lvova,
  • I. E. Shohin,
  • L. A. Menshikova,
  • T. N. Komarov,
  • Yu. E. Boldina,
  • Yu. V. Medvedev

Journal volume & issue
Vol. 0, no. 1
pp. 100 – 104

Abstract

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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, analytical range. It was shown than main validation characteristics meet the Russian State Pharmacopoeia requirements.

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