Results 221 to 230 of about 53,339 (246)
Some of the next articles are maybe not open access.

Thirteen years of medication alerts issued by the Brazilian Health Regulatory Agency (ANVISA): What is the profile?

Journal of Evaluation in Clinical Practice, 2020
RATIONALE, AIMS, AND OBJECTIVES As a pharmacovigilance measure, the Brazilian Health Regulatory Agency (ANVISA) monitors the postmarketing events of medication and issues alerts on actions to be taken and information updates.
Vitor Costa Ferreira   +2 more
exaly   +5 more sources

Do surgimento ao ocaso da anuência prévia da Anvisa: uma análise crítica do patenteamento farmacêutico no Brasil

Revista Digital De Direito Administrativo
The article aims to develop a critical and historical analysis of the prior consent of patents for pharmaceutical products and processes by the Brazilian Health Regulatory Agency (Anvisa) from its creation until its extinction.
Allan Fuezi Barbosa   +2 more
exaly   +2 more sources

ASPECTOS LEGAIS QUANTO AO GERENCIAMENTO DE RESÍDUOS DE SERVIÇOS DE SAÚDE (RSS): ESTUDO COMPARADO ENTRE A RDC ANVISA NO 222/2018 E A RDC ANVISA NO 306/2004

open access: yesRevista Eletrônica de Gestão e Tecnologias Ambientais, 2020
Os residuos de servicos de saude (RSS) sao reconhecidos por sua periculosidade e consequencias associadas ao manejo inadequado, necessitando, assim, de regulamentacao e controle.
Adílio Campos Portugal, L. R. Moraes
semanticscholar   +3 more sources

Vitamin Dietary Supplement: Changes and Challenges with the New ANVISA Regulations [PDF]

open access: yesInternational Journal of Nutrology, 2021
AbstractIn July 2018, the Brazilian National Health Surveillance Agency (Agência Nacional de Vigilância Sanitária, ANVISA, in Portuguese) published new regulations for food supplements, leading to changes both in the sales denomination and labeling statements, and in the composition of these products.
Lucile Tiemi Abe-matsumoto
exaly   +3 more sources

A produção normativa das agências reguladoras: limites para eventual controle da atuação regulatória da Anvisa em resposta à Covid-19

Revista de informacao legislativa, 2021
Este artigo tem por objetivo analisar a produção normativa da Anvisa em resposta à crise de saúde pública gerada pelo novo coronavírus. Com base em levantamento das medidas regulatórias adotadas pela Agência entre os meses de janeiro a junho de 2020 ...
Natasha Schmitt Caccia Salinas   +2 more
semanticscholar   +1 more source

The context and quality of evidence used by tobacco interests to oppose ANVISA’s 2012 regulations in Brazil

open access: yesGlobal Public Health, 2018
Evidence is an important resource for policy makers. Alongside its practical utility, evidence is a persuasive strategic and rhetorical tool. This study scrutinises the information used by tobacco interests in opposition to Brazil's National Health Surveillance Agency's (ANVISA) 2012 regulations.
R. Lencucha, Clelio de Lima Pontes
semanticscholar   +3 more sources

Should ANVISA be permitted to reject pharmaceutical patent applications in Brazil?

Expert Opinion on Therapeutic Patents, 2014
Pharmaceutical manufacturers who seek new markets for expansion are particularly attracted to Brazil given its potential for growth and the expectation that it will be the fifth largest drug market by 2015. Given the significance of Brazil in the marketplace, strong patent protection for pharmaceutical products and processes is critical. In April 2013,
Lisa Mueller   +1 more
semanticscholar   +4 more sources

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