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Trial Registration for Public Trust: Making the Case for Medical Devices

Recently, several pharmaceutical companies have been shown to have withheld negative clinical trial results from the public. These incidents have resulted in a concerted global effort to register all trials at inception, so that all subsequent results can be tracked regardless of whether they are po...

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Detalles Bibliográficos
Autor principal: Sim, Ida
Formato: Texto
Lenguaje:English
Publicado: Springer-Verlag 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2150638/
https://www.ncbi.nlm.nih.gov/pubmed/18095047
http://dx.doi.org/10.1007/s11606-007-0300-7
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author Sim, Ida
author_facet Sim, Ida
author_sort Sim, Ida
collection PubMed
description Recently, several pharmaceutical companies have been shown to have withheld negative clinical trial results from the public. These incidents have resulted in a concerted global effort to register all trials at inception, so that all subsequent results can be tracked regardless of whether they are positive or negative. These trial registration policies have been driven in large part by concern about the pharmaceutical sector. The medical device industry is much smaller, and different from the pharmaceutical industry in some fundamental ways. This paper examines the issues surrounding registration of device trials and argues that these differences with pharmaceutical should not exempt device trials from registration.
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spelling pubmed-21506382008-05-06 Trial Registration for Public Trust: Making the Case for Medical Devices Sim, Ida J Gen Intern Med Perspectives Recently, several pharmaceutical companies have been shown to have withheld negative clinical trial results from the public. These incidents have resulted in a concerted global effort to register all trials at inception, so that all subsequent results can be tracked regardless of whether they are positive or negative. These trial registration policies have been driven in large part by concern about the pharmaceutical sector. The medical device industry is much smaller, and different from the pharmaceutical industry in some fundamental ways. This paper examines the issues surrounding registration of device trials and argues that these differences with pharmaceutical should not exempt device trials from registration. Springer-Verlag 2007-12-19 2008-01 /pmc/articles/PMC2150638/ /pubmed/18095047 http://dx.doi.org/10.1007/s11606-007-0300-7 Text en © Society of General Internal Medicine 2007
spellingShingle Perspectives
Sim, Ida
Trial Registration for Public Trust: Making the Case for Medical Devices
title Trial Registration for Public Trust: Making the Case for Medical Devices
title_full Trial Registration for Public Trust: Making the Case for Medical Devices
title_fullStr Trial Registration for Public Trust: Making the Case for Medical Devices
title_full_unstemmed Trial Registration for Public Trust: Making the Case for Medical Devices
title_short Trial Registration for Public Trust: Making the Case for Medical Devices
title_sort trial registration for public trust: making the case for medical devices
topic Perspectives
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2150638/
https://www.ncbi.nlm.nih.gov/pubmed/18095047
http://dx.doi.org/10.1007/s11606-007-0300-7
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