Federal procurement of unlicensed medicines in Brazil; findings and implications

Author:

Teodoro Cristiane Roberta dos Santos1,Caetano Rosângela2,Godman Brian345,dos Reis André Luís Almeida6,Maia Aurélio de Araújo7,Ramos Mariana de Carvalho Barbosa7,Osorio-de-Castro Claudia Garcia Serpa1

Affiliation:

1. Department of Pharmaceutical Policies and Pharmaceutical Services, Sergio Arouca National School of Public Health, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil

2. Social Medicine Institute, Rio de Janeiro State University, Rio de Janeiro, Brazil

3. Strathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, Glasgow, UK

4. Division of Clinical Pharmacology, Karolinska Institutet, Stockholm, Sweden

5. Liverpool Health Economics Centre, University of Liverpool Management School, Liverpool, UK

6. Coordination of Intellectual Property, Brazilian National Regulatory Agency (ANVISA), Rio de Janeiro, Brazil

7. Department of Health Economics, Investment and Development, Executive Secretariat, Brazilian Ministry of Health, Brasília, Brazil

Funder

Brazilian Research and Development Council

Publisher

Informa UK Limited

Subject

Pharmacology (medical),Health Policy,General Medicine

Reference32 articles.

1. Dabigatran – a case history demonstrating the need for comprehensive approaches to optimize the use of new drugs

2. Risk of cardiovascular events and rofecoxib: cumulative meta-analysis

3. Dabigatran: how the drug company withheld important analyses

4. Examples of how the pharmaceutical industries distort the evidence of drug safety: the case of pioglitazone and the bladder cancer issue

5. Brasil. Lei Federal n° 6.360, de 23 de setembro de 1976. Diário Oficial da União 1976. [Federal Law number 6360, Sept 23 1976. Brazilian National Gazette 1976]. Portuguese. 1976. [cited 2016 Mar 16]. Available from: www.planalto.gov.br/ccivil_03/leis/l6360.htm

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