Results 21 to 30 of about 1,345 (192)

In Vitro Comparative Quality Assessment of Different Brands of Doxycycline Hyclate Finished Dosage Forms: Capsule and Tablet in Jimma Town, South‐West Ethiopia

open access: yesAdvances in Pharmacological and Pharmaceutical Sciences, Volume 2021, Issue 1, 2021., 2021
Background. Persistent postmarket quality evaluation helps produce clear information on the current quality status of the different brands of a given drug and hence introduces a biopharmaceutical and therapeutically equivalent list of the products to the prescribers and users of it. This in turn facilitates access to essential medicines by breaking the
Woldemichael Abraham   +4 more
wiley   +1 more source

Comparative analysis of carbomer polymers for pharmaceutical and cosmetic practice

open access: yesZaporožskij Medicinskij Žurnal, 2020
The aim of the study. Given the wide range of carbomers, their manufacturing technologies, solvent systems for their synthesis, differences in name and regulation, there is a need to systematize this group of excipients for the pharmaceutical and ...
H. P. Kukhtenko   +3 more
doaj   +1 more source

Comparative Analysis of Russian and Foreign Pharmacopoeial Requirements for the Quality Control of Water for Injection: Challenges and Ways of Harmonisation

open access: yesБиопрепараты: Профилактика, диагностика, лечение, 2019
Parenteral dosage forms are dissolved using sterile water for injection whose quality is regulated by special requirements. The lack of a monograph on sterile water for injection in the State Pharmacopoeia of the Russian Federation, as well as the ...
S. M. Sukhanova, N. M. Minaeva
doaj   +1 more source

Obtaining the Enoxaparin Sodium Substance Equivalent to the Original Clexane® and Lovenox®. The Selection of Technological Parameters and Optimization of the “Greenness” of the Purification Stage

open access: yesЖурнал органічної та фармацевтичної хімії, 2023
The aim of the study was to adjust and optimize the purification stage of crude enoxaparin sodium to obtain a substance equivalent to the original drugs Clexane® and Lovenox® according to the criteria specified by the FDA. The purification stage involves
Yuliia V. Bovsunovska   +4 more
doaj   +1 more source

APPROACHES TO THE STANDARDIZATION OF THE CHAMOMILE FLOWERS (CHAMOMILLAE RECUTITA FLORES) IN THE RUSSIAN AND FOREIGN PHARMACOPOEIAS

open access: yesФармация и фармакология (Пятигорск), 2017
The article describes approaches to standardization of chamomile flowers in European Pharmacopoeia, British Pharmacopoeia, United States Pharmacopoeia, and State Pharmacopoeia thirteenth edition (SP XIII).The aim of this work is to analyze the quality ...
E. Y. Zagorulko, M. G. Ozhigova
doaj   +1 more source

Quality of fixed dose artemether/lumefantrine products in Jimma Zone, Ethiopia [PDF]

open access: yes, 2019
Background: Malaria caused by Plasmodium vivax and Plasmodium falciparum is among the major public health problems in most endemic areas of the world.
Bayisa, Bikila   +10 more
core   +1 more source

Pharmacopeial aspects of preparation of infusions and decoctions in pharmacies [PDF]

open access: yes, 2021
An analytical review of pharmacopoeial aspects of preparation of infusions and decoctions in pharmacies is presented. The aim of this work is to conduct a comparative analysis of pharmacopoeial requirements for the technology of infusions and decoctions ...
Buryak, Marina   +2 more
core   +3 more sources

Methodological Approaches to Determination of Depressor Substances in Medicinal Products

open access: yesРегуляторные исследования и экспертиза лекарственных средств, 2020
In order to harmonise national and foreign requirements for quality control of medicinal products, a second variant of the test method, which complies with the requirements of the European Pharmacopoeia, was included into the general monograph OFS.1.2.4 ...
T. A. Batuashvili   +3 more
doaj   +1 more source

Content uniformity of quartered hydrocortisone tablets in comparison with mini-tablets for paediatric dosing [PDF]

open access: yes, 2018
Objectives Children requiring cortisol replacement therapy are often prescribed hydrocortisone doses of 2.5 mg, but as this is commercially unavailable 10 mg tablets, with functional break lines, are split commonly in an attempt to deliver the correct ...
Blair, J   +5 more
core   +1 more source

Comparative analysis of quality attributes of a human albumin preparation with a modified stabilising composition

open access: yesБиопрепараты: Профилактика, диагностика, лечение, 2023
Scientific relevance. The national and international human albumin preparations registered in the Russian Federation mainly differ in their excipient compositions.
M. V. Tomilin   +2 more
doaj   +1 more source

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