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Strategies for ensuring quality data from Indian investigational sites

The topic of ensuring quality and compliance is and must be a top priority in the conduct of clinical trials, as warranted by regulatory guidelines as well as the inherent responsibility of the professionals conducting such research. Fast-growing emerging clinical geographies such as India demand sp...

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Detalles Bibliográficos
Autores principales: Hajos, Antal K., Kamble, Sujal K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3121264/
https://www.ncbi.nlm.nih.gov/pubmed/21731855
http://dx.doi.org/10.4103/2229-3485.80367
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author Hajos, Antal K.
Kamble, Sujal K.
author_facet Hajos, Antal K.
Kamble, Sujal K.
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description The topic of ensuring quality and compliance is and must be a top priority in the conduct of clinical trials, as warranted by regulatory guidelines as well as the inherent responsibility of the professionals conducting such research. Fast-growing emerging clinical geographies such as India demand special attention due to rapid growth and associated factors that may put study quality at risk. In this paper, we used the basic principle of PDCA (Plan, Do, Check, and Adjust) to structure the processes of a clinical trial from protocol to final analysis in order to highlight the interactive nature of involved people and processes required to ensure quality of data and site functioning.
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spelling pubmed-31212642011-07-01 Strategies for ensuring quality data from Indian investigational sites Hajos, Antal K. Kamble, Sujal K. Perspect Clin Res Quality The topic of ensuring quality and compliance is and must be a top priority in the conduct of clinical trials, as warranted by regulatory guidelines as well as the inherent responsibility of the professionals conducting such research. Fast-growing emerging clinical geographies such as India demand special attention due to rapid growth and associated factors that may put study quality at risk. In this paper, we used the basic principle of PDCA (Plan, Do, Check, and Adjust) to structure the processes of a clinical trial from protocol to final analysis in order to highlight the interactive nature of involved people and processes required to ensure quality of data and site functioning. Medknow Publications 2011 /pmc/articles/PMC3121264/ /pubmed/21731855 http://dx.doi.org/10.4103/2229-3485.80367 Text en © Perspectives in Clinical Research http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Quality
Hajos, Antal K.
Kamble, Sujal K.
Strategies for ensuring quality data from Indian investigational sites
title Strategies for ensuring quality data from Indian investigational sites
title_full Strategies for ensuring quality data from Indian investigational sites
title_fullStr Strategies for ensuring quality data from Indian investigational sites
title_full_unstemmed Strategies for ensuring quality data from Indian investigational sites
title_short Strategies for ensuring quality data from Indian investigational sites
title_sort strategies for ensuring quality data from indian investigational sites
topic Quality
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3121264/
https://www.ncbi.nlm.nih.gov/pubmed/21731855
http://dx.doi.org/10.4103/2229-3485.80367
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