Results 1 to 10 of about 35,166 (233)
Регуляторные исследования и экспертиза лекарственных средств, 2018 Russian requirements for main products derived from human plasma used to be laid out in several nonintegrated monographs that have been recently included into the State Pharmacopoeia of the Russian Federation, XIII edition.
A. V. Karyakin, E. D. Skotselyas
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The state pharmacopoeia in the system of higher education
Регуляторные исследования и экспертиза лекарственных средств, 2018 The article provides with a brief historical background for the editions of the State Pharmacopoeia. It characterizes the Russian State Pharmacopoeia of the XIII edition.
I. I. Krasnyuk, N. B. Demina
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TABLETS. REGULATORY REQUIREMENTS OF THE STATE PHARMACOPOEIA XIII EDITION
Разработка и регистрация лекарственных средств, 2019 Comparative analysis of pharmacopoeial requirements for dosage forms tablets has been made due to the introduction of the State Pharmacopoeia of the Russian Federation XIII edition. An overview of changed requirements can be useful for revision (reissue)
N. V. Isaeva +2 more
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The History of the Creation of the VII State Pharmacopoeia of the USSR (Review)
Разработка и регистрация лекарственных средств, 2021 Introduction. The objective necessity of the appearance of this code of laws for the pharmaceu-tical industry is shown. The proofs of the readiness of all branches of pharmacy to develop the text of the Pharmacopoeia, taking into account modern ...
K. S. Guzev
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Биопрепараты: Профилактика, диагностика, лечение, 2022 To ensure the safety and to secure the approval of injectable medicinal products based on antigen-specific immunoglobulins of animal origin, it is necessary to exclude their contamination with adventitious human pathogens.
V. V. Mashin +6 more
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Pharmaceutical Substances. Requirements of the State Pharmacopoeia for Their Standardization
Антибиотики и Химиотерапия, 2020 The present article reviews the modern approaches for the standardization of synthetic pharmaceutical substances that are realized in the form of national pharmacopoeial standards - monographs published in State Pharmacopoeia of Russian Federation.
E. I. Sakanyan +4 more
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Open Access Journal of Pharmaceutical Research, 2023 The objective of the study is to ensure Indian pharmacopoeia monographs are on par with United States, British pharmacopoeia standards. A few monographs were selected on random and compared. It has been observed that Indian pharmacopoeia has replaced titrimetrry assay method of analysis to sophisticated chromatographic techniques.
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Rupture Test and Bioavailability of Oil-Soluble Vitamins [PDF]
, 2013 In lieu of an abstract, here is the article\u27s first paragraph: Bioavailability of multi-vitamins as dietary supplements has always been a concern. Dissolution studies have been successfully used to predict drug release of bioactive molecules, but with
Chablani, Lipika
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Experimental Study of Antimicrobial Properties and Acute Toxicity of the Peo-based Combined Suppositories [PDF]
, 2019 Aim. The research of antimicrobial and toxicological parameters of a promising pharmaceutical composition with indole-3-carbinol and meloxicam in the form of rectal suppositories.Materials and methods.
Ravshanov, T. (Tymur) +4 more
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Регуляторные исследования и экспертиза лекарственных средств, 2020 The study of the nomenclature of officinal herbal substances and medicinal plants is important for finding potential ways of expanding the existing range of raw materials used in the production of herbal medicinal products.
L. N. Frolova +5 more
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