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1

Relevant Issues of Planning Bioequivalence Studies of Drugs with a Narrow Therapeutic Range

Relevant Issues of Planning Bioequivalence Studies of Drugs with a Narrow Therapeutic Range

Por D. P. Romodanovsky
Publicado em 2020-09-01

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2

Alternative Methods for Dissolution Profile Comparison in the Dissolution Test

Por D. P. Romodanovsky, D. V. Goryachev
Publicado em 2021-11-01

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3

Expert Approaches to the Assessment of Losartan Drugs Bioequivalence

Expert Approaches to the Assessment of Losartan Drugs Bioequivalence

Por D. P. Romodanovsky, D. V. Goryachev
Publicado em 2020-02-01

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4

Planning and evaluation of bioequivalence studies of rosuvastatin drug products

Planning and evaluation of bioequivalence studies of rosuvastatin drug products

Por D. P. Romodanovsky, D. V. Goryachev
Publicado em 2018-02-01

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5

Planning and Evaluation of Bioequivalence Studies of Telmisartan Generic Drug Products

Planning and Evaluation of Bioequivalence Studies of Telmisartan Generic Drug Products

Por A. L. Khokhlov, D. P. Romodanovsky, A. E. Miroshnikov
Publicado em 2019-09-01

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6

Planning Bioequivalence Studies in the Context of the COVID-19 Pandemic

Planning Bioequivalence Studies in the Context of the COVID-19 Pandemic

Por D. P. Romodanovsky, A. L. Khokhlov, D. V. Goryachev
Publicado em 2021-03-01

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7

Regulatory requirements of the European Medicines Agency for evaluation of bioequivalence of modified-release medicinal products

Regulatory requirements of the European Medicines Agency for evaluation of bioequivalence of modified-release medicinal products

Por D. P. Romodanovsky, N. N. Eremenko, D. V. Goryachev
Publicado em 2019-03-01

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8

PRINCIPLES OF STATISTICAL EVALUATION OF BIOEQUIVALENCE STUDIES IN THE CONTEXT OF CURRENT REGULATORY REQUIREMENTS AND LEGAL ACTS

PRINCIPLES OF STATISTICAL EVALUATION OF BIOEQUIVALENCE STUDIES IN THE CONTEXT OF CURRENT REGULATORY REQUIREMENTS AND LEGAL ACTS

Por D. P. Romodanovsky, D. V. Goryachev, A. P. Solovieva, N. N. Eremenko
Publicado em 2018-06-01

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9

EXPERT APPROACHES TO EQUIVALENCE EVALUATION OF DRUGS — ANALOGUES OF ENDOGENOUS COMPOUNDS AS CONSISTENT WITH THE RUSSIAN LEGISLATION AND INTERNATIONAL LAW

EXPERT APPROACHES TO EQUIVALENCE EVALUATION OF DRUGS — ANALOGUES OF ENDOGENOUS COMPOUNDS AS CONSISTENT WITH THE RUSSIAN LEGISLATION AND INTERNATIONAL LAW

Por D. P. Romodanovsky, D. V. Goryachev, A. P. Solovieva, I. V. Kokin, N. N. Eremenko
Publicado em 2018-03-01

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10

Highly variable medicines - specific aspects of bioequivalence studies

Highly variable medicines - specific aspects of bioequivalence studies

Por D. P. Romodanovsky, T. V. Eremenkova, M. A. Dranitsyna, D. V. Goryachev, R. R. Niyazov, E. V. Gavrishina, V. A. Merkulov
Publicado em 2018-02-01

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11

PRECLINICAL AND CLINICAL ASPECTS OF THE DEVELOPMENT OF BIOMEDICAL CELL PRODUCTS

PRECLINICAL AND CLINICAL ASPECTS OF THE DEVELOPMENT OF BIOMEDICAL CELL PRODUCTS

Por A. V. Tikhomirova, D. V. Goryachev, V. A. Merkulov, I. V. Lysikova, A. I. Gubenko, A. I. Zebrev, А. P. Solovieva, D. P. Romodanovsky, E. V. Melnikova
Publicado em 2018-03-01

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