USE OF DISSOLUTION TEST FOR EVALUATION OF PHARMACEUTICAL EQUIVALENCE OF ATORVASTATIN GENERICS by O. V. Druzhininskaya, I. E. Smekhova

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DISSOLUTION MEDIA USED IN DEVELOPMENT AND QUALITY CONTROL OF DRUGS by O. V. Druzhininskaya, I. E. Smekhova

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Choice of Extraction Method for Receiving Extraction from Seeds of Payne Hay with the High Content of Biologically Active Substances by S. S. Belokurov, E. V. Flysyuk, I. E. Smekhova

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DISSOLUTION PROFILE STUDIES FOR RAMIPRIL AND LERCANIDIPINE FIXED-DOSE COMBINATION by A. A. Shadrin, E. V. Flisyuk, I. E. Smekhova

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Transfer of Cosmetic Emulsion Cream Technology from Laboratory to Pilot Phase by M. A. Burakova, O. N. Abrosimova, Yu. M. Ladutko, I. E. Smekhova

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Documentation of Pharmaceutical Development. Part 1. Study of the Documentation of the Site by I. E. Smekhova, L. V. Shigarova, V. D. Meteleva, E. V. Flisyuk

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Application of Quality-by-Design Approach to Justify the Composition and Technology of Two-component Suppositories by I. E. Smekhova, L. V. Shigarova, P. I. Andreeva, E. V. Flisyuk, A. S. Dzyuba

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Documentation of Pharmaceutical Development. Part 2. Quality System Documents by I. E. Smekhova, L. V. Shigarova, I. A. Narkevich, E. V. Flisyuk, V. D. Meteleva

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Development of the "Dissolution" Test Method for Tablets of Sodium 4,4'-(propanediamido)dibenzoate with Sustained Release by E. V. Flisyuk, Ju. M. Kotsur, I. A. Narkevich, I. E. Smekhova, D. Yu. Ivkin

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DISINTEGRANTS AND THEIR INFLUENCE ON THE DISSOLUTION OF SUBSTANCES OF BIOPHARMACEUTICAL CLASSIFICATION SYSTEM CLASSES by I. E. Smekhova, V. A. Vainshtein, Y. M. Ladutko, O. V. Druzhininskaya, N. N. Tureckova

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Study of Lercanidipine Drug Release from Medicine in Combination with Ramipril <i>in vitro</i> and <i>in vivo by A. A. Shadrin, D. Y. Ivkin, E. V. Flisyuk, I. E. Smekhova, G. A. Plisko, A. A. Karpov, E. D. Semivelichenko

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