Inertial regimes of viscous fluid flow in the low-height cylinder with rotating bases by V. K. Akhmetov, Yu. V. Medvedev, V. Ya. Shkhadov

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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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The determination of topiramate in plasma rabbit blood by HPLC with specific derivatization by G. V. Ramenskaya, M. A. Sheveleva, I. E. Shokhin, Yu. V. Medvedev, T. A. Yarushok

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Development and validation of the methods for determination of tenophovir in the blood plasma of rabbits by Yu. V. Medvedev, G. V. Ramenskaya, I. E. Shokhin, T. A. Yarushok, M. A. Sheveleva

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

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Erratum: "HPLC-UV Method Development and Validation for Vitamin D₃ (Cholecalciferol) Quantitationin 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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DISSOLUTION PROFILE STUDY FOR EXTENDED RELEASE VALPROIC ACID DOSAGE FORM (DEPAKINE® CHRONO) by A. A. Lvova, Yu. E. Boldina, I. E. Shohin, T. N. Komarov, L. A. Menshikova, Yu. V. Medvedev

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Development and Validation of Valganciclovir and its Active Metabolite Ganciclovir Determination in Human Plasma by HPLC-UV Method by T. N. Komarov, I. E. Shohin, O. A. Miskiv, D. S. Bogdanova, A. V. Aleshina, Yu. V. Medvedev, N. S. Bagaeva

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

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Comparative Analysis of Dalargin Pharmaceutical Substance Identification Methods by M. G. Shulzhenko, I. A. Vasilenko, B. I. Ugrak, I. E. Shohin, Yu. V. Medvedev, E. A. Malashenko

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Immunogenicity Assessment of Pegfilgrastim in Patients with Breast Cancer by Yu. V. Medvedev, M. A. Kolganova, O. A. Sas, T. N. Komarov, E. N. Fisher, I. E. Shohin, Yu. I. Ammour

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Approaches to conducting a physiologically relevant test (PRT) in the study of medicines containing substance IIc of the BCS subclass using sorafenib as an example by A. V. Suvorova, Yu. V. Medvedev, P. A. Losenkova, O. S. Kramarenko, E. A. Malashenko, A. M. Poluyanov, I. E. Shohin

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Development and Validation of Salbutamol, Bromhexine, Ambroxol and Guauaifenesin Determination in Human Plasma by HPLC-MS/MS Method by T. N. Komarov, D. S. Bogdanova, O. A. Miskiv, A. V. Aleshina, I. E. Shohin, Yu. V. Medvedev, N. S. Bagaeva, I. M. Korenskaya

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PRT to predict pharmacokinetic profiles as part of a bioequivalence study of the drug deferasirox by A. V. Suvorova, P. A. Losenkova, Yu. V. Medvedev, E. A. Malashenko, I. E. Makarenko, A. M. Poluyanov, I. E. Shohin

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Chemical and Toxicological Analysis of Antiretroviral Drugs by T. N. Komarov, M. V. Belova, D. D. Stolyarova, I. E. Shohin, D. S. Bogdanova, O. A. Miskiv, Yu. V. Medvedev, I. M. Korenskaya

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Hygienic Monitoring of Working Area Air Pollution by Particulate Matter of ticagrelator in the Pharmaceutical Factory by I. A. Pozharnov, A. S. Simakov, N. A. Shulga, A. Yu. Savchenko, O. I. Perederyaev, L. S. Synkova, Yu. V. Medvedev, E. N. Fisher

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