The 10 references in paper G. Vasilenko F., N. Dubovik S., I. Shohin E., G. Gildeeva N., G. Ramenskaya V., L. Pavlova A., Г. Василенко Ф., Н. Дубовик С., И. Шохин Е., Г. Гильдеева Н., Г. Раменская В., Л. Павлова А. (2018) “Оценка влияния автоматизации на вариабельность результатов теста «Растворение» на примере лекарственного препарата «Бетагистина гидрохлорид таблетки 16 мг» // Assessing the impact of the automation on the variability of the «Dissolution» test results as exemplified by «Betahistine hydrochloride tablets 16 mg»” / spz:neicon:vedomostincesmp:y:2016:i:3:p:53-57

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Ramenskaya GV, Nedogoda SV, Shohin IE, Savchenko AYu, Shlykov VS. Therapeutic drugs and biopharmaceutical evaluation of indapamide. Kardiovaskulyarnaya terapiya i profilaktika 2011;10(8): 105–9 (in Russian).
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Zhang Hua Yu, Lawrence X. Dissolution testing for solid oral drug products: theoretical considerations. Amer Pharm Rev. 2010; (6): 1–4.
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Smehova IE, Perova YuM, Kondratiev IA, Rodygina AN, Turetskova NN. Test «Dissolution» and modern approaches to the assessment of equivalence of drugs. Razrabotka i registratsiya lekarstvennyh sredstv 2013;1(2): 50–60 (in Russian).
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Features of pharmaceutical technological equipment ERWEKA. The development and registration of drugs. Special Issue Analytics EXPO 2013: 6–10 (in Russian).
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Iarriccio A, Kassis A, Patel T. Increasing the Efficiency of the Dissolution Laboratory through Automation. The Review of American Pharmaceutical Business and Technology 2011.
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Kretz J, Wong-Moon K. Evaluation of Automation to Increase Efficiency in the Dissolution Lab. Dissolution Technologies 2013; 20(2): 33–7.
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USP 33 — NF 28. Monograph 1092 «The Dissolution Procedure: Development and Validation».
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State quality standard drug. GPA 42-0003–04 «Dissolution». Moscow; 2004 (in Russian). AUTHORS Federal State Budgetary Institution «Scientific Centre for Expert Evaluation of Medicinal Products» of the Ministry of Health of the Russian Federation, Petrovsky boulevard 8, bld. 2, Moscow 127051, Russian Federation.
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