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Artículo

Medical devices: from licensing to coverage. highlights from Argentina, Brazil, Colombia and Mexico

Rey Ares, Lucila; Hernández Vásquez, Akram; Garay, Osvaldo Ulises; Pichón-Riviere, AndrésIcon ; García Martí, SebastiánIcon ; Gilardino, Ramiro; Cabra, Hermilio Arturo; Augustovski, Federico ArielIcon
Fecha de publicación: 11/2016
Editorial: Expert Reviews
Revista: Expert Review of Medical Devices
ISSN: 1743-4440
Idioma: Inglés
Tipo de recurso: Artículo publicado
Clasificación temática:
Medicina Critica y de Emergencia

Resumen

Objectives: To assess, describe and compare the requirements and pathwaysof medical devices from licensing to coverage in four Latin American countries(LAC) health systems. Methods: We conducted a literature search (February 2015)on Pubmed, Lilacs and Value in Health Regional Issues journal. We also searchedspecific websites of Health Technology Assessment (HTA) and regulatory agencies,ministries of health and health agencies; and a performed generic Internet search.We included all publications describing aspects related to regulation, coverage,medical technology innovation, and HTA and Economic Evaluation (EE) guidelines.We additionally interviewed key informants from all countries to gather informationrelated to the aforementioned processes. We present here the literature searchresults. Results: We included 60 studies out of 2190. Five percent of the publicationsanalyzed the four countries jointly, 75% were from Brazil, 8.3% from Mexico, 5%from Colombia and 5.7% from LAC in general. Half of the studies described the roleof the HTA and EE in decision-making and aspects or policies related to innovation(25% and 23.3%). Regarding the description of the coverage process, it was addressedin 13.3% of the studies; 10% of the publications focused on technovigilance; and also10% on regulatory aspects. Remaining publications were methodological guidelinesand general descriptions of the health systems and the role of medical devices. Allcountries had HTA and EE guidelines, although there did not include device specificrecommendations. There is a spectrum of HTA formalization for technology incorporationafter licensing, higher in Brazil and lower in Argentina Conclusions:There is scarce information on the processes and requirements to achieve coveragefor medical devices in these countries. Processes differ, are in general not explicit,lack transparency, and usually replicate those of drugs not taking into account thespecificities of medical devices.
Palabras clave: Medical Devices , Licensing , Coverage , Reimbursement , Latin America
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info:eu-repo/semantics/openAccess Excepto donde se diga explícitamente, este item se publica bajo la siguiente descripción: Creative Commons Attribution-NonCommercial-ShareAlike 2.5 Unported (CC BY-NC-SA 2.5)
Identificadores
URI: http://hdl.handle.net/11336/47340
DOI: https://dx.doi.org/10.1080/17434440.2016.1245611
URL: https://www.tandfonline.com/doi/full/10.1080/17434440.2016.1245611#
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Citación
Rey Ares, Lucila; Hernández Vásquez, Akram; Garay, Osvaldo Ulises; Pichón-Riviere, Andrés; García Martí, Sebastián; et al.; Medical devices: from licensing to coverage. highlights from Argentina, Brazil, Colombia and Mexico; Expert Reviews; Expert Review of Medical Devices; 13; 11; 11-2016; 1053-1065
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