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A critical assessment of brazil’s emerging pharmaceutical market

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Previous issue date: 2016-11-08 / Brazil has emerged as a leader in new sites selected for clinical trials, by offering a multitude of benefits to sponsors. Even though there are significant delays with regulatory timelines, it provides highly qualified investigators, low costs, a strong infrastructure, well-established ethical support, and high patient recruitment and adherence rates. However, in order to become a primary location for clinical trials, Brazil will have to streamline and improve regulatory processes and the current political and financial conditions. The study was conducted with consensus judgement and analysis of 15 experienced industry reviewers have provided informative descriptive data. The findings suggest areas in new clinical trial in which strategies for workflow and process development could improve efficiency of clinical development.

Identiferoai:union.ndltd.org:IBICT/oai:bibliotecadigital.fgv.br:10438/17977
Date08 November 2016
CreatorsPalmer, Jiibril
ContributorsPinto, Mario Couto Soares, Ferreira, Luís Fernando Filardi, Escolas::EBAPE, Zanini, Marco Túlio Fundão
Source SetsIBICT Brazilian ETDs
LanguageEnglish
Detected LanguageEnglish
Typeinfo:eu-repo/semantics/publishedVersion, info:eu-repo/semantics/masterThesis
Sourcereponame:Repositório Institucional do FGV, instname:Fundação Getulio Vargas, instacron:FGV
Rightsinfo:eu-repo/semantics/openAccess

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