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Impact of regulatory assessment on clinical studies in Brazil

Overview of attention for article published in Revista da Associação Médica Brasileira, August 2016
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Title
Impact of regulatory assessment on clinical studies in Brazil
Published in
Revista da Associação Médica Brasileira, August 2016
DOI 10.1590/1806-9282.62.05.447
Pubmed ID
Authors

Luis Augusto Tavares Russo, Freddy Goldberg Eliaschewitz, Vitor Harada, Roberta Pereira Trefiglio, Raffaella Picciotti, Paula Goulart Pinheiro Machado, Gustavo Luiz Ferreira Kesselring

Abstract

Despite the recent expansion of clinical studies allocated to Brazil, the delay of local regulatory deadlines directly impacts their completion. This article examines the allocation process of clinical studies to Brazil in comparison with other countries, as well as the financial impact of studies not completed due to interruption caused by the delay in the regulatory process. The allocation processes of studies were compared in nine countries with similar stages of economic development and countries in Latin America using the websites http://data.worldbank.org/data-catalog/GDP-rankings-table and http://worldpopulationreview.com and clinicaltrials.gov, comprising 185 countries. The 46 studies sponsored by the pharmaceutical industry underwent an analysis of the regulatory review process. 46 studies sponsored by the industry and submitted in the country between June 2007 and June 2013 were analyzed; 18 (39%) were discontinued due to the delay in obtaining the necessary approvals. For the approved studies, patient recruitment began an average of 11 months after the other countries. It is estimated that 530 Brazilians patients did not have the opportunity to participate in these studies. Financial losses were to the order of 14.6 million dollars for the country, including patient, medication and supplies costs, and expenses. Brazil has enormous potential for the realization of clinical studies. Researchers, associations of disabled people and patients with chronic diseases, sponsors and the authorities must work together to develop an approval process that is efficient, predictable and, most of all, transparent. The current regulatory environment must and can be improved and optimized in order to result in tangible benefits for patients, society and the country's scientific development.

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Mendeley readers

The data shown below were compiled from readership statistics for 30 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
France 1 3%
Unknown 29 97%

Demographic breakdown

Readers by professional status Count As %
Student > Master 8 27%
Student > Postgraduate 3 10%
Researcher 3 10%
Student > Doctoral Student 2 7%
Other 1 3%
Other 4 13%
Unknown 9 30%
Readers by discipline Count As %
Medicine and Dentistry 9 30%
Business, Management and Accounting 3 10%
Philosophy 1 3%
Pharmacology, Toxicology and Pharmaceutical Science 1 3%
Environmental Science 1 3%
Other 5 17%
Unknown 10 33%