A validated stability indicating RP-HPLC method for valganciclovir, identification and characterization of forced degradation products of valganciclovir using LC-MS/MS-Reference-Cited by-同舟云学术

A validated stability indicating RP-HPLC method for valganciclovir, identification and characterization of forced degradation products of valganciclovir using LC-MS/MS

Published:2014-03 Issue:1 Volume:26 Page:29-42
ISSN:1233-2356
Container-title:Acta Chromatographica
language:en
Short-container-title:Acta Chromatographica

Author:

Sawant S.,Barge V.

Publisher

Akademiai Kiado Zrt.

Subject

General Chemistry

Link

https://www.akademiai.com/doi/pdf/10.1556/achrom.26.2014.1.4

Reference17 articles.

1. International Conference on Harmonization (ICH), Q1A (R2): Stability testing of new drug substances and products, IFPMA, Geneva, 2003

2. World Health Organization (WHO): Draft stability testing of active pharmaceutical ingredients and pharmaceutical products, Geneva, 2007

3. Development of validated stability-indicating assay methods—critical review

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