Pharmaceutical Companies vs. the State: Who is Responsible for Post-Trial Provision of Drugs in Brazil?

Author:

Wang Daniel Wei L.,Ferraz Octavio Luiz Motta

Abstract

This paper discusses so-called post-trial access to drugs for patients who participated in clinical trials in Brazil. Brazil is currently a relevant country for the pharmaceutical industry due to the dimensions of its actual and potential market. As a consequence, the number of pharmaceutical trials has been rising. It is the largest market for pharmaceutical companies in Latin America, the 8th biggest in the world and second only to China among the so-called BRICS’s emerging countries. The demand for pharmaceutical products in the country has been increasing by double digits over the last few years, reaching 20% in 2008. Not surprisingly, we are also witnessing a steady increase in the number of applications by national and international pharmaceutical companies before ethical research authorities for authorization to perform clinical trials of drugs.

Publisher

Cambridge University Press (CUP)

Subject

Health Policy,General Medicine,Issues, ethics and legal aspects

Reference58 articles.

1. 42 Article IV.1. Our free translation, from Portuguese, that reads as follows: L - Assegurar por parte do patrocinador ou, na sua inexistência, por parte da instituição, pesquisador ou promotor, acesso ao medicamento em teste, caso se comprove sua superioridade em relação ao tratamento convencional.

2. 41 The Brazilian National Health Council. Resolution 196/1996, at Article III.3.

3. 46 Brazil, , Federal Constitution at Article 196, available at (last visited May 22, 2012).

4. 24 World Medical Association, Declaration of Helsinki, 2000, available at (last visited May 22, 2012).

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