Relevant Issues of Planning Bioequivalence Studies of Drugs with a Narrow Therapeutic Range von Romodanovsky, D. P.

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Alternative Methods for Dissolution Profile Comparison in the Dissolution Test von Romodanovsky, D. P., Goryachev, D. V.

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Planning Bioequivalence Studies in the Context of the COVID-19 Pandemic von Romodanovsky, D. P., Khokhlov, A. L., Goryachev, D. V.

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Expert Approaches to the Assessment of Losartan Drugs Bioequivalence von Romodanovsky, D. P., Goryachev, D. V.

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Regulatory Requirements of the European Medicines Agency for Evaluation of Bioequivalence of Modified-release Medicinal Products von Romodanovsky, D. P., Eremenko, N. N., Goryachev, D. V.

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INFLUENCE OF SEX DIFFERENCES ON PHARMACOKINETICS OF DRUGS WITHIN THE FRAMEWORK OF BIOEQUIVALENCE STUDIES OF GENERIC MEDICINAL PRODUCTS von Romodanovsky, D. P., Goryachev, D. V., Khokhlov, A. L., Miroshnikov, A. E.

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PRINCIPLES OF STATISTICAL EVALUATION OF BIOEQUIVALENCE STUDIES IN THE CONTEXT OF CURRENT REGULATORY REQUIREMENTS AND LEGAL ACTS von Romodanovsky, D. P., Goryachev, D. V., Solovieva, A. P., Eremenko, N. N.

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EXPERT APPROACHES TO EQUIVALENCE EVALUATION OF DRUGS — ANALOGUES OF ENDOGENOUS COMPOUNDS AS CONSISTENT WITH THE RUSSIAN LEGISLATION AND INTERNATIONAL LAW von Romodanovsky, D. P., Goryachev, D. V., Solovieva, A. P., Kokin, I. V., Eremenko, N. N.

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PRECLINICAL AND CLINICAL ASPECTS OF THE DEVELOPMENT OF BIOMEDICAL CELL PRODUCTS von Tikhomirova, A. V., Goryachev, D. V., Merkulov, V. A., Lysikova, I. V., Gubenko, A. I., Zebrev, A. I., Solovieva, А. P., Romodanovsky, D. P., Melnikova, E. V.

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lanning and Evaluation of Bioequivalence Studies of Telmisartan Generic Drug Products von Khokhlov, A. L., Romodanovsky, D. P., Miroshnikov, A. E.

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Planning and Evaluation of Bioequivalence Studies of Telmisartan Generic Drug Products von A. L. Khokhlov, D. P. Romodanovsky, A. E. Miroshnikov

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