Regulations, conflicts and ethics of medical research in developing countries

Authors

  • Marta Maciel Lyra Cabral Fundação Oswaldo Cruz; Departamento de Imunologia
  • Haiana Charifker Schindler Fundação Oswaldo Cruz; Departamento de Imunologia
  • Frederico Guilherme Coutinho Abath Fundação Oswaldo Cruz; Departamento de Imunologia

DOI:

https://doi.org/10.1590/S0034-89102006000300022

Keywords:

Clinical trials^i2^seth, Ethics, research, Ethics committees, Biomedical research^i2^seth, Human experimentation^i2^seth, Developing countries

Abstract

The patient is the subject who may meet the needs and interests of medical investigators for their research. This intrinsic conflict becomes more evident and shows particularities in the context of research projects involving clinical trials in developing countries. Target populations in these countries have inadequate access to health services, little understanding of risks involved in a study and also less capacity to claim judicially in the event of damage. In general, the discussions on ethics in research in industrialized countries are characterized by a biomedical approach of disease, and a neoliberal vision of economy and trade. In fact, most biomedical research has been directed to benefit already privileged communities. Therefore, it is necessary to minimize the risk of exploitation of developing countries populations. The present study provides an outlook of ethical protection for human research in developing countries.

Published

2006-06-01

Issue

Section

Commentary

How to Cite

Cabral, M. M. L., Schindler, H. C., & Abath, F. G. C. (2006). Regulations, conflicts and ethics of medical research in developing countries . Revista De Saúde Pública, 40(3), 521-527. https://doi.org/10.1590/S0034-89102006000300022