USE OF DISSOLUTION TEST FOR EVALUATION OF PHARMACEUTICAL EQUIVALENCE OF ATORVASTATIN GENERICS

by O. V. Druzhininskaya, I. E. Smekhova
Published 2019-01-01

DISSOLUTION MEDIA USED IN DEVELOPMENT AND QUALITY CONTROL OF DRUGS

by O. V. Druzhininskaya, I. E. Smekhova
Published 2019-01-01

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
Published 2019-09-01

DISSOLUTION PROFILE STUDIES FOR RAMIPRIL AND LERCANIDIPINE FIXED-DOSE COMBINATION

by A. A. Shadrin, E. V. Flisyuk, I. E. Smekhova
Published 2019-01-01

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
Published 2021-02-01

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
Published 2021-05-01

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
Published 2019-01-01

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
Published 2019-09-01