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CTRI – Clicking to greater transparency and accountability

A clinical trial registry (CTR) is an official platform for registering a clinical trial (CT) with an objective of providing increased transparency and access to CTs to the public at large. Clinical Trials Registry - India (CTRI) is a free online public record system for registration of CTs being co...

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Detalles Bibliográficos
Autor principal: George, Bobby
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3530978/
https://www.ncbi.nlm.nih.gov/pubmed/23293758
http://dx.doi.org/10.4103/2229-3485.103592
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author George, Bobby
author_facet George, Bobby
author_sort George, Bobby
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description A clinical trial registry (CTR) is an official platform for registering a clinical trial (CT) with an objective of providing increased transparency and access to CTs to the public at large. Clinical Trials Registry - India (CTRI) is a free online public record system for registration of CTs being conducted in India. The vision of the CTRI is to ensure that every CT conducted in the region is prospectively registered with full disclosure of the trial data set items. With more number of CTs being conducted in the country, with a large number being global multicentre trials, it is binding on the industry/investigators/sponsor to comply with the requirements laid down. While there are pros and cons, there is enough scope for improvement of CTRI.
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spelling pubmed-35309782013-01-04 CTRI – Clicking to greater transparency and accountability George, Bobby Perspect Clin Res Review Article A clinical trial registry (CTR) is an official platform for registering a clinical trial (CT) with an objective of providing increased transparency and access to CTs to the public at large. Clinical Trials Registry - India (CTRI) is a free online public record system for registration of CTs being conducted in India. The vision of the CTRI is to ensure that every CT conducted in the region is prospectively registered with full disclosure of the trial data set items. With more number of CTs being conducted in the country, with a large number being global multicentre trials, it is binding on the industry/investigators/sponsor to comply with the requirements laid down. While there are pros and cons, there is enough scope for improvement of CTRI. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3530978/ /pubmed/23293758 http://dx.doi.org/10.4103/2229-3485.103592 Text en Copyright: © Perspectives in Clinical Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
George, Bobby
CTRI – Clicking to greater transparency and accountability
title CTRI – Clicking to greater transparency and accountability
title_full CTRI – Clicking to greater transparency and accountability
title_fullStr CTRI – Clicking to greater transparency and accountability
title_full_unstemmed CTRI – Clicking to greater transparency and accountability
title_short CTRI – Clicking to greater transparency and accountability
title_sort ctri – clicking to greater transparency and accountability
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3530978/
https://www.ncbi.nlm.nih.gov/pubmed/23293758
http://dx.doi.org/10.4103/2229-3485.103592
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