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Biomedical Chromatography : BMC|December 11, 2023
Stability indicating reversed-phase-high-performance liquid chromatography method development and validation for pyridostigmine bromide and sodium benzoate in oral solutionVaishnavi ChintalaBiomedical Chromatography : BMC|March 12, 2025
Stability-Indicating RP-HPLC Method Development and Validation for Determination of Impurities in Loperamide Hydrochloride Capsules Dosage FormSreenivas Pippalla, Vaishnavi ChintalaJournal of Separation Science|December 22, 2023
A quality-by-design evaluated liquid chromatography method development and validation for the separation and quantification of nitroxoline and its impuritiesSanthi Priya Lankalapalli, K Vijaya Rachel, Vaishnavi Chintala, et al.ACS Omega|March 25, 2024
Quality by Design Tool Assessed Ultraperformance Liquid Chromatography Method for the Analysis of Remogliflozin and Teneligliptin in Oral Dosage FormJyothsna Menda, Vaishnavi Chintala, Phani Raja Kanuparthy, et al.Journal of AOAC International|September 27, 2023
Quantification of Drospirenone- and Ethinyl Estradiol-Related Impurities in a Combined Pharmaceutical Dosage Form by a Chromatography Method With a QbD Robustness StudySrinivasa Reddy Chinta, Vaishnavi Chintala, Vishnu Nandimalla, et al.Pageof 1