Regulation of health products: Striving for best practices

Authors

  • Daniela Trejos Vargas Pontifícia Universidade Católica do Rio de Janeiro, Rio de Janeiro/RJ

DOI:

https://doi.org/10.11606/issn.2316-9044.v18i2p112-121

Keywords:

Brazilian Health Regulatory Agency, Health Regulation.

Abstract

The section "Argument" on this issue of the Revista de Direito Sanitário (Journal of Health Law) is again centered on the existing regulatory framework of Brazil in the area of health products. The three articles selected bring an approach with a comparative bias in the different areas in which the Brazilian Health Regulatory Agency (Anvisa) operates: regulation of medical supplies, analysis and registration of pharmaceutical patents and ex post facto control of medicines dangerousness through recall.

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Author Biography

  • Daniela Trejos Vargas, Pontifícia Universidade Católica do Rio de Janeiro, Rio de Janeiro/RJ

    PhD in Civil Law by Universidade do Estado do Rio de Janeiro (UERJ); master in Constitutional Law by Pontifícia Universidade Católica do Rio de Janeiro (PUC-Rio); bachelor’s degree in Law by PUC-Rio. Coordinator of the Bachelor’s degree at Centro de Ciências Sociais da PUC-Rio; professor at graduation and post graduation at PUC-Rio; member of the Núcleo de Direitos Humanos at PUC-Rio.

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Published

12/26/2017

Issue

Vol. 18 No. 2 (2017)

Section

Argument

License

The Revista de Direito Sanitário/ Journal of Health Law adopts the conditions of the Creative Commons Attribution 4.0 Internacional. This license allows to share - "copy and redistribute the material in any medium or format for any purpose, even commercially" and adapt - "remix, transform, and build upon the material for any purpose, even commercially." Details at: https://creativecommons.org/licenses/by/4.0/deed.en

How to Cite

Vargas, D. T. (2017). Regulation of health products: Striving for best practices. Journal of Health Law, 18(2), 112-121. https://doi.org/10.11606/issn.2316-9044.v18i2p112-121