DEVELOPMENT, VALIDATION AND APPLICATION OF ANTI-Xa- AND ANTI-IIa-ENOXAPARINE SODIUM ASSAY by B. Yu. Margaeva, I. E. Shohin

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EVALUATION OF THE AUTOMATION INFLUENCE ON THE DISSOLUTION VARIABILITY RESULTS FOR BETASERC TABLETS by N. S. Dubovik, I. E. Shohin, L. A. Pavlova

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AN EXPERIENCE OF IMPLEMENTING LIMS SYSTEM IN THE BIOANALYTICAL LABORATORY (PART 1) by A. A. Krylatova, I. E. Shohin, A. S. Kardashin

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CERTIFICATION OF QUALITY MANAGEMENT SYSTEM OF LLC «CENTER OF PHARMACEUTICAL ANALYTICS» ACCORDING TO THE REQUIREMENTS OF ISO 9001:2015 (GOST R ISO 9001-2015) (REVIEW) by A. A. Krylatova, I. E. Shohin, E. P. Obrazcova

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MODERN APPROACHES OF DISSOLUTION PROFILE TEST (REVIEW) by D. Yu. Grebenkin, Ya. M. Stanishevskiy, I. E. Shohin

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Method of Estimating the Equivalence of Dissolution Profiles: a Modern View (Review) by I. E. Shohin, N. S. Bagaeva, E. A. Malashenko, V. N. Kuzina

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EXPERIENCE OF CERTIFICATION BIOANALYTICAL LABORATORY ACCORDING TO REQUIREMENTS OF GOST 33044-2014 «PRINCIPLES OF GOOD LABORATORY PRACTICE» (GLP) by A. A. Krylatova, I. E. Shohin, E. P. Obrazcova, A. O. Monaenkov

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RETROSPECTIVE OF DISSOLUTION TEST OF SOLID DOSAGE FORMS (REVIEW) by D. Yu. Grebenkin, Ya. M. Stanishevskiy, I. E. Shohin, E. A. Malashenko

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Biowaiver as a Bioequivalence Study Option by E. A. Volkova, Yu. V. Medvedev, E. N. Fisher, I. E. Shohin

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PD-L1 as a Potential Target in Cancer Therapy (Review) by N. N. Andrusova, M. A. Kolganova, A. V. Aleshina, I. E. Shohin

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DETERMINATION OF CAPECITABINE AND ITS ACTIVE METABOLITE 5-FLUOROURACIL IN BLOOD PLASMA BY HPLC-MS/MS by E. S. Melnikov, I. E. Shohin, A. A. Aksenov, G. V. Adamov, A. N. Konyushkova

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DISSOLUTION PROFILE STUDY FOR INNOVATION ANTI-RETROVIRAL DRUG PRODUCT NIKAVIR® AND ITS FIXED COMBINATION WITH LAMIVUDINE (PHOSPHALADINE®) by I. E. Shohin, Yu. V. Medvedev, T. N. Komarov, O. V. Klimova, B. V. Brovchenko

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Development and Validation of Tadalafil Determination in Human Plasma by HPLC-MS Method by D. S. Bogdanova, T. N. Komarov, I. E. Shohin, E. S. Melnikov, O. A. Miskiv, Yu. V. Medvedev

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Phase I Pharmacokinetics Study of Oral Administration of Esperavir® (INN: Molnupiravir) (LLC "PROMOMED RUS", Russia) by T. N. Komarov, N. S. Bagaeva, K. K. Karnakova, K. Ya. Zaslavskaya, P. A. Bely, I. E. Shohin

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Phase I Pharmacokinetics Study of Drug for Infusion «Areplivir» (INN: Favipiravir) (LLC "PROMOMED RUS", Russia) by T. N. Komarov, N. S. Bagaeva, K. K. Karnakova, I. E. Shohin, K. Ya. Zaslavskaya, P. A. Bely

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Erratum: "Development, Validation and Approbation Analytical Method for the Quantitative Determination of Taurine by HPLC-UV Method in the Test of Comparative Dissolution Kinetics" by A. M. Poluyanov, A. Kochug, L. S. Mitrofanova, I. D. Nikitin, O. Yu. Vergasov, I. E. Shohin

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HPLC-MS/MS method development and validation for the determination of tetradecapeptide in human plasma by M. A. Tokareva, E. S. Melnikov, M. V. Belova, E. N. Fisher, T. A. Rodina, I. E. Shohin

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Assessing the impact of the automation on the variability of the «Dissolution» test results as exemplified by «Betahistine hydrochloride tablets 16 mg» by G. F. Vasilenko, N. S. Dubovik, I. E. Shohin, G. N. Gildeeva, G. V. Ramenskaya, L. A. Pavlova

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VALIDATION OF UV-SPECTROMETRY ASSAY METHOD FOR DISSOLUTION PROFILE TEST FOR LEVOFLOXACINE TABLETS by A. A. Lvova, I. E. Shohin, L. A. Menshikova, T. N. Komarov, Yu. E. Boldina, Yu. V. Medvedev

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HPLC-UV Method Development and Validation for Vitamin D₃ (Cholecalciferol) Quantitation in Drugs and Dietary Supplements by I. E. Shohin, E. A. Malashenko, Yu. V. Medvedev, M. N. Bogachuk, S. A. Kulakov, M. A. Paleeva

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