Lei da fosfoetanolamina sintética no Brasil

Luana Dias Costa; Sandra Mara Campos Alves

doi:10.17566/ciads.v7i1.468

Vol. 7 No. 1 (2018), ARTICLES

Vol. 7 No. 1 (2018)

Synthetic phosphoethanolamine law in Brazil

ARTICLES

Published 2018-04-02

Luana Dias Costa⁺⁻
Sandra Mara Campos Alves⁺⁻

Luana Dias Costa

Escola Fiocruz de Governo (EFG)

Sandra Mara Campos Alves

Fundação Oswaldo Cruz, Brasília, Brasil.

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Supplementary Files

Anexo (Portuguese)

Keywords

Brazilian Health Surveillance Agency
Government Regulation
Judiciary

DOI:

https://doi.org/10.17566/ciads.v7i1.468

How to Cite

1.

Synthetic phosphoethanolamine law in Brazil. Cad. Ibero Am. Direito Sanit. [Internet]. 2018 Apr. 2 [cited 2025 Apr. 30];7(1):215-28. Available from: https://www.cadernos.prodisa.fiocruz.br/index.php/cadernos/article/view/468

Abstract

Objective: The objective was to analyze the context in which the aforementioned law was proposed and approved, in light of Brazilian legislation. Methodology: This was a descriptive-analytical study, considering that a theoretical review of the information available on the House Bill PL 4.639 / 2016, Federal Senate PLC No. 3/2016 and the Law of Phosphoethanolamine, Law 13,269, of April 13, 2016, in addition to the normative review of the attributions and competencies of Brazilian Health Surveillance Agency. Results: It is clear that a whole legal framework has been replaced by ordinary legislation with concrete effects. Conclusions: In the case in question, Brazilian Health Surveillance Agency performance was disregarded, since it is up to the Agency to carry out all the tests and subsequently release the product for consumption.

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This work is licensed under a Creative Commons Attribution 4.0 International License.

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