Zobrazeno 1 - 10
of 75
pro vyhledávání: '"BIO-EQUIVALENCE"'
Publikováno v:
Quality of Life Research, 1996 Feb 01. 5(1), 20-26.
Externí odkaz:
https://www.jstor.org/stable/4034776
Publikováno v:
Clinical Pharmacology: Advances and Applications, Vol Volume 8, Pp 191-198 (2016)
Mervyn Mer,1 Jacques Rene Snyman,2 Constance Elizabeth Jansen van Rensburg,2 Jacob John van Tonder,3 Ilze Laurens2 1Department of Medicine, Divisions of Critical Care and Pulmonology, University of the Witwatersrand, Johannesburg, South Africa; 2Offi
Externí odkaz:
https://doaj.org/article/245fd308512944d2b486f2efd5e621bf
Publikováno v:
Journal of Scientific Research and Reports. :123-130
A crossover design is a repeated measurements design such that each experimental unit receives different treatments during the different time periods. In a majority of bioequivalence studies, design and analysis of cross-over using classical methods
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b5562536974c415a12db471a37260495
https://doi.org/10.9734/jsrr/2021/v27i930440
https://doi.org/10.9734/jsrr/2021/v27i930440
Publikováno v:
International Journal of Research in Pharmaceutical Sciences. 12:1478-1483
The work aims to develop an appropriate method for mexiletine with 35-65% recovery by the LPE method with efficient and selective efficacy of the IS and analyte for the analysis under Liquid Chromatography-Mass Spectrometry/ Mass Spectrometry. This m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::62319f94bed37bd6337ea936c38ea3e5
https://doi.org/10.26452/ijrps.v12i2.4718
https://doi.org/10.26452/ijrps.v12i2.4718
Autor:
Holger Dette, Kevin Kokot
Publikováno v:
Biometrika. 108:895-913
Summary We study the problem of testing equivalence of functional parameters, such as the mean or the variance function, in the two-sample functional data setting. In contrast to previous work where the functional problem is reduced to a multiple tes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be0f5e3a6d7e6a452ae77949498745ff
https://doi.org/10.1093/biomet/asaa096
https://doi.org/10.1093/biomet/asaa096
Autor:
Eric Yining Qi, Daohong Chen
Publikováno v:
Translational Research
Clinical trials serve as the gold standard to evaluate the efficacy and safety of tested drugs prior to marketing authorization. Nevertheless, there have been a few challenging issues well noted in traditional clinical trials such as tedious processi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87a6c949f82efa428525578f3acbced5
https://doi.org/10.1016/j.trsl.2020.05.007
https://doi.org/10.1016/j.trsl.2020.05.007
Autor:
Mohamed Aboubakr, Ashraf Elkomy
Publikováno v:
International Journal of Advanced Research. 8:152-157
The present study was designed to assess the comparative bio-equivalence of Micotil 300? and Cozina 300? in healthy Calves after SC injection of both products in a dose of 10 mg tilmicosin base/kg.b.wt. Ten calves were divided equally into two groups
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e3bd23e6aaac4b0dca477ad7396473c
https://doi.org/10.21474/ijar01/10609
https://doi.org/10.21474/ijar01/10609
Autor:
Rhian Jaymar D. Ramil, Jan Karlo T. Ecalne, Benjel Andaya Andaya, Gerard Q. de Guzman, Ma. Danica I. Ramil
Publikováno v:
Advance Pharmaceutical Journal. 3:62-69
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b9895f0e5f26dac2b1896427e352f7e5
https://doi.org/10.31024/apj.2018.3.2.4
https://doi.org/10.31024/apj.2018.3.2.4
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