Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Monika Marczak"'
Autor:
Tomasz Grabowski, Monika Marczak
Publikováno v:
Letters in Drug Design & Discovery. 13:422-428
Publikováno v:
International Journal of Pharmacokinetics. 1:9-11
Autor:
Tomasz Grabowski, Jerzy Jan Jaroszewski, Krystyna Okoniewska, Jakub Okoniewski, Monika Marczak
Publikováno v:
Bulletin of the Veterinary Institute in Pulawy, Vol 59, Iss 3, Pp 383-391 (2015)
The aim of this study was to determine the correlation between lipophilicity and maximum residue limit (MRL) value specified for veterinary drugs in the fatty tissue of various animal species. The analysis was performed on a group of 73 compounds wit
Publikováno v:
Drug Research. 65:410-415
During the past years, a growing number of bacterial strains have become resistant to tetracyclines. The problem of increasing resistance and lack of susceptibility to tetracyclines applies to strains isolated from both: animals and humans. Basic too
Autor:
Monika Marczak
Publikováno v:
Polish Journal of Social Rehabilitation, Vol 3, Pp 63-72 (2012)
The underlining arguement in this article is to highlight the positive effect of comunity service as a form of punishment for criminal activity, which other than a fine is considered the lightest form of penalty. This is because it does not take the
Autor:
Tomasz, Grabowski, Monika, Marczak, Miroslaw, Muszynski, Muszynski, Miroslaw, Jerzy Jan, Jaroszewski
Publikováno v:
Bioanalysis. 4:417-430
This article is an attempt to present issues associated with the principles of GLP system harmonization, particularly in relation to pharmacokinetic (PK) studies at a global scale. Complete harmonization of GLP principles requires unification at seve
Akademický článek
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Publikováno v:
Regulatory toxicology and pharmacology : RTP. 64(2)
Guidelines published by the European Union Regulatory Authority, regarding the planning of bioequivalence studies, are the primary source of knowledge about the study design optimization. The goal of this paper is to compare the key elements (27 poin
Publikováno v:
In Silico Pharmacology
Background Total body clearance of biological drugs is for the most part dependent on the receptor mechanisms (receptor mediated clearance) and the concentration of antibodies aimed at administered drug – anti-drug-antibodies (ADA). One of the sign