Results 11 to 20 of about 1,256,119 (263)

POST-MARKETING DRUG SAFETY RESEARCH: ANALYSIS OF RECOMMENDATIONS OF FOREIGN REGULATORS

open access: yesБезопасность и риск фармакотерапии, 2018
The monitoring of information on the safety of various drugs is becoming more relevant day by day, as the number of drugs on the  pharmaceutical market increases, generic drugs, bio-analogous drugs appear.
E. V. Shubnikova   +8 more
doaj   +1 more source

Pharmacogenetic Approaches to Enhancing Efficacy and Safety of Statins as Illustrated by the Example of Atorvastatin

open access: yesБезопасность и риск фармакотерапии, 2020
Statins are efficacious lipid-lowering drugs used for prevention of cardiovascular complications in patients with high blood cholesterol. The efficacy and safety of this group of drugs is largely determined by genetic factors. The aim of the study was to
R. Ye. Kazakov   +7 more
doaj   +1 more source

Experience with the use of pharmacopoeial reference material for the activity of measles vaccine

open access: yesВопросы вирусологии, 2023
Introduction. Due to the increased incidence of measles in Russia and in many other regions of the world, vaccines for the measles prevention are especially in demand. Ensuring the quality of the measles vaccine for effective disease prevention is within
Anna S. Binyatova   +6 more
doaj   +1 more source

Scientific Collaboratories: Evaluating their Potential [PDF]

open access: yesBulletin of the American Society for Information Science and Technology, 2002
L'auteur presente une evaluation ayant pour but de repondre aux questions suivantes: la recherche scientifique repartie (laboratoire virtuel) peut-elle produire des resultats de qualite elevee? les avantages des labos virtuels compenssent-ils les inconvenients, selon les scientifiques eux-memes?
Sonnenwald, Diane H.   +2 more
openaire   +1 more source

Evaluating Scientific Content

open access: yesThe American Biology Teacher, 2013
An evaluation of the scientific content in a popular children’s movie about bees provides an opportunity for discussion about the sources and consequences of scientific misconceptions.
Heather Worsham, Lauren Diepenbrok
openaire   +1 more source

Nonspecific Impurities in Pharmaceutical Substances: Characteristics of Test Methods

open access: yesРегуляторные исследования и экспертиза лекарственных средств, 2019
One of the prerequisites of efficacy and safety of finished pharmaceutical products is the quality of pharmaceutical substances used in their production.
Yu. R. Biglova   +8 more
doaj   +1 more source

International Approaches to Regulation of Medicinal Products Containing Viable Human Cells

open access: yesБиопрепараты: Профилактика, диагностика, лечение, 2018
The intensive development of cellular technologies stipulates the introduction at the global level of medicinal products based on viable human cells, which in most countries are referred to as biomedical cell products. The authors conducted a comparative
E. V. Melnikova   +8 more
doaj   +1 more source

Post-approval variations to dossiers for vaccines: analysis of regulatory and methodological approaches used in the Russian Federation and abroad

open access: yesРегуляторные исследования и экспертиза лекарственных средств, 2019
The management of post-approval changes to registration dossiers for medicinal products is one of the most important factors for ensuring sustainable quality, safety and efficacy of medicines.
V. A. Shevtsov   +8 more
doaj   +1 more source

Comparative Dissolution Kinetics of Several Multisource Thioctic Acid Products

open access: yesРегуляторные исследования и экспертиза лекарственных средств, 2022
The relationship between dissolution and bioavailability is an example of the interdependency between the quality of a medicinal product and its safety and efficacy.
G. F. Vasilenko   +6 more
doaj   +1 more source

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