{"id":3339,"date":"2021-12-17T12:53:49","date_gmt":"2021-12-17T12:53:49","guid":{"rendered":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/training-and-capacity-building-resources\/regulator-sessions\/serie-de-seminarios-web-sobre-uso-de-normas-consensuadas-voluntarias\/"},"modified":"2022-04-04T17:52:26","modified_gmt":"2022-04-04T17:52:26","slug":"serie-de-seminarios-web-sobre-uso-de-normas-consensuadas-voluntarias","status":"publish","type":"regulator-sessions","link":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/training-and-capacity-building-resources\/regulator-sessions\/serie-de-seminarios-web-sobre-uso-de-normas-consensuadas-voluntarias\/?lang=es","title":{"rendered":"Serie de Seminarios Web sobre Uso de Normas Consensuadas Voluntarias"},"content":{"rendered":"\n

El Proyecto de Convergencia Regulatoria de Dispositivos M\u00e9dicos<\/a> co-liderado por USAID, ANSI, y AdvaMed a trav\u00e9s de la Coalici\u00f3n Interamericana para la Convergencia Regulatoria<\/a> en el Sector de Tecnolog\u00eda M\u00e9dica, en colaboraci\u00f3n con la Administraci\u00f3n de Alimentos y Medicamentos de los Estados Unidos (USFDA) han organizado una serie de sesiones web sobre la utilizaci\u00f3n de Normas Internacionales con prop\u00f3sitos regulatorios.<\/p>\n\n\n\n

Sesi\u00f3n I. 7 Diciembre de 2021<\/strong><\/h2>\n\n\n\n

Objectivo<\/strong>: Proporcionar la experiencia de USFDA en el Desarrollo y aplicaci\u00f3n de las normas consensuadas al tomar decisiones regulatorias que promueven la seguridad y efectividad de los dispositivos m\u00e9dicos.<\/p>\n\n\n\n

Agenda<\/h2>\n\n\n\n
\n
Ingl\u00e9s<\/a><\/div>\n\n\n\n
Espa\u00f1ol<\/a><\/div>\n\n\n\n
Portugu\u00e9s<\/a><\/div>\n<\/div>\n\n\n\n

Grabaci\u00f3n<\/h2>\n\n\n\n
\n
Ingl\u00e9s<\/a><\/div>\n\n\n\n
Espa\u00f1ol<\/a><\/div>\n\n\n\n
Portugu\u00e9s<\/a><\/div>\n<\/div>\n\n\n\n

Presentacion<\/h2>\n\n\n\n
\n
Ingl\u00e9s<\/a><\/div>\n\n\n\n
Espa\u00f1ol<\/a><\/div>\n\n\n\n
Portugu\u00e9s<\/a><\/div>\n<\/div>\n\n\n\n

Sesi\u00f3n II. 3 Marzo 2022<\/strong><\/h2>\n\n\n\n

Objetivo<\/strong>: Proporcionar las perspectivas de la OPS\/OMS, , OMC y las Organizaciones Desarrolladoras de Normas (ODN) sobre c\u00f3mo los reguladores y la industria desarrollan, mantienen y utilizan normas voluntarias consensuadas internacionalmente para tecnolog\u00edas m\u00e9dicas, con el prop\u00f3sito de poner en pr\u00e1ctica \u201creliance\u201d regulatorio, la convergencia regulatoria y facilitar la fabricaci\u00f3n y aprobaci\u00f3n de dispositivos m\u00e9dicos de calidad, seguros, interoperables, eficaces y accesibles para los sistemas de salud y accesibles para los pacientes en las Am\u00e9ricas.<\/p>\n\n\n\n

Agenda<\/h2>\n\n\n\n
\n
Ingl\u00e9s<\/a><\/div>\n\n\n\n
Espa\u00f1ol<\/a><\/div>\n\n\n\n
Portugu\u00e9s<\/a><\/div>\n<\/div>\n\n\n\n

Grabaci\u00f3n<\/h2>\n\n\n\n
\n
Ingl\u00e9s<\/a><\/div>\n\n\n\n
Espa\u00f1ol<\/a><\/div>\n\n\n\n
Portugu\u00e9s<\/a><\/div>\n<\/div>\n\n\n\n

Presentaciones<\/h2>\n\n\n\n

Parte 1. El uso de las normas internacionales para las tecnolog\u00edas m\u00e9dicas como clave para la aplicaci\u00f3n de \u201cReliance\u201d, la convergencia regulatoria y el cumplimiento legal<\/strong><\/h3>\n\n\n\n

Referencias sanitarias para Autoridades Regulatorias Nacionales de Dispositivos M\u00e9dicos – Alexandre Lemgruber, PAHO<\/h4>\n\n\n\n
\n
Ingl\u00e9s<\/a><\/div>\n\n\n\n
Espa\u00f1ol<\/a><\/div>\n\n\n\n
Portugu\u00e9s<\/a><\/div>\n<\/div>\n\n\n\n

Obligaciones Legales aplicables a Autoridades Nacionales Regulaatorias de Dispositivos M\u00e9dicos – Acuerdo de Obst\u00e1culos T\u00e9cnicos al Comercio – Devin McDaniels, OMC<\/h4>\n\n\n\n
\n
Ingl\u00e9s<\/a><\/div>\n\n\n\n
Espa\u00f1ol<\/a><\/div>\n\n\n\n
Portugu\u00e9s<\/a><\/div>\n<\/div>\n\n\n\n

Obligaciones Legales aplicables a Autoridades Regulatorias de Dispositivos M\u00e9dicos – Renata Amaral, IACRC<\/h4>\n\n\n\n
\n
Ingl\u00e9s<\/a><\/div>\n\n\n\n
Espa\u00f1ol<\/a><\/div>\n\n\n\n
Portugu\u00e9s<\/a><\/div>\n<\/div>\n\n\n\n

Normas Internacionales – Desarrollo, Adopci\u00f3n y Utilizaci\u00f3n por los Actores Interesados, inclyendo a las Autoridades Regulatorias – Kory Eguino, COPANT<\/h4>\n\n\n\n
\n
Ingl\u00e9s<\/a><\/div>\n\n\n\n
Espa\u00f1ol<\/a><\/div>\n\n\n\n
Portugu\u00e9s<\/a><\/div>\n<\/div>\n\n\n\n

Parte 2. Panel de Discusi\u00f3n: Panorama General del Trabajo de las Organizaciones Desarrolladoras de Normas en el \u00e1rea de Technolog\u00eda M\u00e9dica<\/strong><\/h3>\n\n\n\n

ISO \/ TC210 – Peter Linders, Philips<\/h4>\n\n\n\n
\n
Ingl\u00e9s<\/a><\/div>\n\n\n\n
Espa\u00f1ol<\/a><\/div>\n\n\n\n
Portugu\u00e9s<\/a><\/div>\n<\/div>\n\n\n\n

Grupo de Trabajo de Traducciones al Espa\u00f1ol ISO \/ TC210 – Veronica Viscovich, IRAM<\/h4>\n\n\n\n
\n
Ingl\u00e9s<\/a><\/div>\n\n\n\n
Espa\u00f1ol<\/a><\/div>\n\n\n\n
Portugu\u00e9s<\/a><\/div>\n<\/div>\n\n\n\n

IEC \/ TC 62 \u2013Brodie Pedersen<\/h4>\n\n\n\n
\n
Ingl\u00e9s<\/a><\/div>\n\n\n\n
Espa\u00f1ol<\/a><\/div>\n\n\n\n
Portugu\u00e9s<\/a><\/div>\n<\/div>\n\n\n\n

IMDRF y Normas \u2013 Kenneth Cavanaugh, USFDA<\/h4>\n\n\n\n
\n
Ingl\u00e9s<\/a><\/div>\n\n\n\n
Espa\u00f1ol<\/a><\/div>\n\n\n\n
Portugu\u00e9s<\/a><\/div>\n<\/div>\n\n\n\n

AAMI \u2013 Hae Choe<\/h4>\n\n\n\n
\n
Ingl\u00e9s<\/a><\/div>\n\n\n\n
Espa\u00f1ol<\/a><\/div>\n\n\n\n
Portugu\u00e9s<\/a><\/div>\n<\/div>\n\n\n\n

CLSI & ISO TC212 \u2013 Patrick McGinn<\/h4>\n\n\n\n
\n
Ingl\u00e9s<\/a><\/div>\n\n\n\n
Espa\u00f1ol<\/a><\/div>\n\n\n\n
Portugu\u00e9s<\/a><\/div>\n<\/div>\n\n\n\n

MITA \u2013 Carolyn Hull<\/h4>\n\n\n\n
\n
Ingl\u00e9s<\/a><\/div>\n\n\n\n
Espa\u00f1ol<\/a><\/div>\n\n\n\n
Portugu\u00e9s<\/a><\/div>\n<\/div>\n\n\n\n

ASTM International \u2013 Craig Updyke<\/h4>\n\n\n\n
\n
Ingl\u00e9s<\/a><\/div>\n\n\n\n
Espa\u00f1ol<\/a><\/div>\n\n\n\n
Portugu\u00e9s<\/a><\/div>\n<\/div>\n\n\n\n

Sesi\u00f3n III, 10 Marzo 2022<\/strong><\/h2>\n\n\n\n

Objetivo<\/strong>: Proporcionar las perspectivas de los Organismos Nacionales de Normalizaci\u00f3n (ONN) sobre c\u00f3mo los reguladores y la industria desarrollan, mantienen y utilizan normas voluntarias consensuadas internacionalmente para tecnolog\u00edas m\u00e9dicas para poner en pr\u00e1ctica \u201creliance\u201d regulatorio, la convergencia regulatoria y facilitar la fabricaci\u00f3n y aprobaci\u00f3n de dispositivos m\u00e9dicos de calidad, seguros, inter operables, eficaces y accesibles para los sistemas de salud y accesibles para los pacientes en las Am\u00e9ricas.<\/p>\n\n\n\n

Agenda<\/h2>\n\n\n\n
\n
Ingl\u00e9s<\/a><\/div>\n\n\n\n
Espa\u00f1ol<\/a><\/div>\n\n\n\n
Portugu\u00e9s<\/a><\/div>\n<\/div>\n\n\n\n

Grabaci\u00f3n<\/h2>\n\n\n\n
\n
Ingl\u00e9s<\/a><\/div>\n\n\n\n
Espa\u00f1ol<\/a><\/div>\n\n\n\n
Portugu\u00e9s<\/a><\/div>\n<\/div>\n\n\n\n

Presentaciones<\/h2>\n\n\n\n

Brazil<\/strong><\/h3>\n\n\n\n

ABNT, Jorge Cajazeira, Assesor de \u00c1rea Internacional<\/h4>\n\n\n\n
\n
Ingl\u00e9s<\/a><\/div>\n\n\n\n
Espa\u00f1ol<\/a><\/div>\n\n\n\n
Portugu\u00e9s<\/a><\/div>\n<\/div>\n\n\n\n

CB-036,Humberto Tiburcio, SBAC<\/h4>\n\n\n\n
\n
Ingl\u00e9s<\/a><\/div>\n\n\n\n
Espa\u00f1ol<\/a><\/div>\n\n\n\n
Portugu\u00e9s<\/a><\/div>\n<\/div>\n\n\n\n

Colombia<\/strong><\/h3>\n\n\n\n

ICONTEC \u2013 Andr\u00e9s Hern\u00e1ndez<\/h4>\n\n\n\n
\n
Ingl\u00e9s<\/a><\/div>\n\n\n\n
Espa\u00f1ol<\/a><\/div>\n\n\n\n
Portugu\u00e9s<\/a><\/div>\n<\/div>\n\n\n\n

Mexico<\/strong><\/h3>\n\n\n\n

DGN \u2013 Emeterio Mosso<\/h4>\n\n\n\n
\n
Ingl\u00e9s<\/a><\/div>\n\n\n\n
Espa\u00f1ol<\/a><\/div>\n\n\n\n
Portugu\u00e9s<\/a><\/div>\n<\/div>\n\n\n\n

ANCE \u2013 Luis Iv\u00e1n Hern\u00e1ndez Becerril<\/h4>\n\n\n\n
\n
Ingl\u00e9s<\/a><\/div>\n\n\n\n
Espa\u00f1ol<\/a><\/div>\n\n\n\n
Portugu\u00e9s<\/a><\/div>\n<\/div>\n\n\n\n

Peru<\/strong><\/h3>\n\n\n\n

INACAL \u2013 Soraya Lastra<\/h4>\n\n\n\n
\n
Ingl\u00e9s<\/a><\/div>\n\n\n\n
Espa\u00f1ol<\/a><\/div>\n\n\n\n
Portugu\u00e9s<\/a><\/div>\n<\/div>\n\n\n\n

Sesi\u00f3n IV. 17 Marzo 2022<\/strong><\/h2>\n\n\n\n

Objetivo<\/strong>: Proporcionar las perspectivas de las autoridades gubernamentales, la industria y el sector de evaluaci\u00f3n de la conformidad y la industria sobre c\u00f3mo la evaluaci\u00f3n de la conformidad es una herramienta global utilizada por los reguladores y la industria para demostrar el cumplimiento de los requisitos \u2013 facilitando la fabricaci\u00f3n y aprobaci\u00f3n de dispositivos m\u00e9dicos de calidad, seguros, interoperables, eficaces y accesibles para los sistemas de salud y los pacientes en las Am\u00e9ricas.<\/p>\n\n\n\n

Agenda<\/h2>\n\n\n\n
\n
Ingl\u00e9s<\/a><\/div>\n\n\n\n
Espa\u00f1ol<\/a><\/div>\n\n\n\n
Portugu\u00e9s<\/a><\/div>\n<\/div>\n\n\n\n

Grabaci\u00f3n<\/h2>\n\n\n\n
\n
Ingl\u00e9s<\/a><\/div>\n\n\n\n
Espa\u00f1ol<\/a><\/div>\n\n\n\n
Portugu\u00e9s<\/a><\/div>\n<\/div>\n\n\n\n

Presentaciones<\/h2>\n\n\n\n

Parte I<\/strong><\/h3>\n\n\n\n

Evaluaci\u00f3n de la Conformidad como Recurso Esencial para las Autoridades Regulatorias de Dispositivos M\u00e9dicos, Industria y Convergencia Regulatoria<\/strong><\/h4>\n\n\n\n

Visi\u00f3n general de la evaluaci\u00f3n de conformidad y la utilizaci\u00f3n gubernamental de CA: Gordon Gillerman, NIST<\/h4>\n\n\n\n
\n
Ingl\u00e9s<\/a><\/div>\n\n\n\n
Espa\u00f1ol<\/a><\/div>\n\n\n\n
Portugu\u00e9s<\/a><\/div>\n<\/div>\n\n\n\n

MedTech Experiencia de la industria con CA: Elisabeth George, Philips<\/h4>\n\n\n\n
\n
Ingl\u00e9s<\/a><\/div>\n\n\n\n
Espa\u00f1ol<\/a><\/div>\n\n\n\n
Portugu\u00e9s<\/a><\/div>\n<\/div>\n\n\n\n

Perspectiva Sectorial de la Evaluaci\u00f3n de la Conformidad: Martin Michelot, Consejo TIC<\/h4>\n\n\n\n
\n
Ingl\u00e9s<\/a><\/div>\n\n\n\n
Espa\u00f1ol<\/a><\/div>\n\n\n\n
Portugu\u00e9s<\/a><\/div>\n<\/div>\n\n\n\n

Esquema IECEE CB: Steven Margis. UL<\/h4>\n\n\n\n
\n
Ingl\u00e9s<\/a><\/div>\n\n\n\n
Espa\u00f1ol<\/a><\/div>\n\n\n\n
Portugu\u00e9s<\/a><\/div>\n<\/div>\n\n\n\n

Parte II<\/strong><\/h3>\n\n\n\n

Mesa redonda: Utilizaci\u00f3n de Normas Internacionales y Evaluaci\u00f3n de la Conformidad por las Autoridades Regulatorias Nacionales de Dispositivos M\u00e9dicos<\/strong><\/h4>\n\n\n\n

Colombia<\/strong><\/h4>\n\n\n\n

Ministerio de Salud, Soleiny Mar\u00edn Cort\u00e9s<\/h4>\n\n\n\n
\n
Ingl\u00e9s<\/a><\/div>\n\n\n\n
Espa\u00f1ol<\/a><\/div>\n\n\n\n
Portugu\u00e9s<\/a><\/div>\n<\/div>\n\n\n\n

INVIMA \u2013 Eleonora Celis Ca\u00f1as<\/h4>\n\n\n\n
\n
Ingl\u00e9s<\/a><\/div>\n\n\n\n
Espa\u00f1ol<\/a><\/div>\n\n\n\n
Portugu\u00e9s<\/a><\/div>\n<\/div>\n\n\n\n

M\u00e9xico<\/strong><\/h4>\n\n\n\n

COFEPRIS \u2013 Llaneth Bola\u00f1os Valerio<\/h4>\n\n\n\n
\n
Ingl\u00e9s<\/a><\/div>\n\n\n\n
Espa\u00f1ol<\/a><\/div>\n\n\n\n
Portugu\u00e9s<\/a><\/div>\n<\/div>\n\n\n\n

FEUM \u2013 Rafael Hern\u00e1ndez<\/h4>\n\n\n\n
\n
Ingl\u00e9s<\/a><\/div>\n\n\n\n
Espa\u00f1ol<\/a><\/div>\n\n\n\n
Portugu\u00e9s<\/a><\/div>\n<\/div>\n","protected":false},"parent":0,"template":"","event_category":[],"class_list":["post-3339","regulator-sessions","type-regulator-sessions","status-publish","hentry","description-off"],"acf":[],"yoast_head":"\nSerie de Seminarios Web sobre Uso de Normas Consensuadas Voluntarias - Regulatory Convergence<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/training-and-capacity-building-resources\/regulator-sessions\/serie-de-seminarios-web-sobre-uso-de-normas-consensuadas-voluntarias\/?lang=es\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Serie de Seminarios Web sobre Uso de Normas Consensuadas Voluntarias - Regulatory Convergence\" \/>\n<meta property=\"og:description\" content=\"El Proyecto de Convergencia Regulatoria de Dispositivos M\u00e9dicos co-liderado por USAID, ANSI, y AdvaMed a trav\u00e9s de la Coalici\u00f3n Interamericana para la Convergencia Regulatoria en el Sector de Tecnolog\u00eda M\u00e9dica, en colaboraci\u00f3n con la Administraci\u00f3n de Alimentos y Medicamentos de los Estados Unidos (USFDA) han organizado una serie de sesiones web sobre la utilizaci\u00f3n de Normas Internacionales con prop\u00f3sitos…\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/training-and-capacity-building-resources\/regulator-sessions\/serie-de-seminarios-web-sobre-uso-de-normas-consensuadas-voluntarias\/?lang=es\" \/>\n<meta property=\"og:site_name\" content=\"Regulatory Convergence\" \/>\n<meta property=\"article:modified_time\" content=\"2022-04-04T17:52:26+00:00\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data1\" content=\"4 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/www.interamericancoalition-medtech.org\\\/regulatory-convergence\\\/training-and-capacity-building-resources\\\/regulator-sessions\\\/serie-de-seminarios-web-sobre-uso-de-normas-consensuadas-voluntarias\\\/?lang=es\",\"url\":\"https:\\\/\\\/www.interamericancoalition-medtech.org\\\/regulatory-convergence\\\/training-and-capacity-building-resources\\\/regulator-sessions\\\/serie-de-seminarios-web-sobre-uso-de-normas-consensuadas-voluntarias\\\/?lang=es\",\"name\":\"Serie de Seminarios Web sobre Uso de Normas Consensuadas Voluntarias - Regulatory Convergence\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/www.interamericancoalition-medtech.org\\\/regulatory-convergence\\\/?lang=es\\\/#website\"},\"datePublished\":\"2021-12-17T12:53:49+00:00\",\"dateModified\":\"2022-04-04T17:52:26+00:00\",\"breadcrumb\":{\"@id\":\"https:\\\/\\\/www.interamericancoalition-medtech.org\\\/regulatory-convergence\\\/training-and-capacity-building-resources\\\/regulator-sessions\\\/serie-de-seminarios-web-sobre-uso-de-normas-consensuadas-voluntarias\\\/?lang=es#breadcrumb\"},\"inLanguage\":\"en-US\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\\\/\\\/www.interamericancoalition-medtech.org\\\/regulatory-convergence\\\/training-and-capacity-building-resources\\\/regulator-sessions\\\/serie-de-seminarios-web-sobre-uso-de-normas-consensuadas-voluntarias\\\/?lang=es\"]}]},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\\\/\\\/www.interamericancoalition-medtech.org\\\/regulatory-convergence\\\/training-and-capacity-building-resources\\\/regulator-sessions\\\/serie-de-seminarios-web-sobre-uso-de-normas-consensuadas-voluntarias\\\/?lang=es#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"Home\",\"item\":\"https:\\\/\\\/www.interamericancoalition-medtech.org\\\/regulatory-convergence\\\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"Regulator Sessions\",\"item\":\"https:\\\/\\\/www.interamericancoalition-medtech.org\\\/regulatory-convergence\\\/training-and-capacity-building-resources\\\/regulator-sessions\\\/\"},{\"@type\":\"ListItem\",\"position\":3,\"name\":\"Serie de Seminarios Web sobre Uso de Normas Consensuadas Voluntarias\"}]},{\"@type\":\"WebSite\",\"@id\":\"https:\\\/\\\/www.interamericancoalition-medtech.org\\\/regulatory-convergence\\\/?lang=es\\\/#website\",\"url\":\"https:\\\/\\\/www.interamericancoalition-medtech.org\\\/regulatory-convergence\\\/?lang=es\\\/\",\"name\":\"Regulatory Convergence\",\"description\":\"Inter-American Coalition\",\"publisher\":{\"@id\":\"https:\\\/\\\/www.interamericancoalition-medtech.org\\\/regulatory-convergence\\\/?lang=es\\\/#organization\"},\"potentialAction\":[{\"@type\":\"SearchAction\",\"target\":{\"@type\":\"EntryPoint\",\"urlTemplate\":\"https:\\\/\\\/www.interamericancoalition-medtech.org\\\/regulatory-convergence\\\/?lang=es\\\/?s={search_term_string}\"},\"query-input\":{\"@type\":\"PropertyValueSpecification\",\"valueRequired\":true,\"valueName\":\"search_term_string\"}}],\"inLanguage\":\"en-US\"},{\"@type\":\"Organization\",\"@id\":\"https:\\\/\\\/www.interamericancoalition-medtech.org\\\/regulatory-convergence\\\/?lang=es\\\/#organization\",\"name\":\"Inter-American Coalition - Regulatory Convergence\",\"url\":\"https:\\\/\\\/www.interamericancoalition-medtech.org\\\/regulatory-convergence\\\/?lang=es\\\/\",\"logo\":{\"@type\":\"ImageObject\",\"inLanguage\":\"en-US\",\"@id\":\"https:\\\/\\\/www.interamericancoalition-medtech.org\\\/regulatory-convergence\\\/?lang=es\\\/#\\\/schema\\\/logo\\\/image\\\/\",\"url\":\"https:\\\/\\\/www.interamericancoalition-medtech.org\\\/regulatory-convergence\\\/wp-content\\\/uploads\\\/sites\\\/4\\\/2021\\\/07\\\/logo_regulatory_retina_en.png\",\"contentUrl\":\"https:\\\/\\\/www.interamericancoalition-medtech.org\\\/regulatory-convergence\\\/wp-content\\\/uploads\\\/sites\\\/4\\\/2021\\\/07\\\/logo_regulatory_retina_en.png\",\"width\":559,\"height\":280,\"caption\":\"Inter-American Coalition - Regulatory Convergence\"},\"image\":{\"@id\":\"https:\\\/\\\/www.interamericancoalition-medtech.org\\\/regulatory-convergence\\\/?lang=es\\\/#\\\/schema\\\/logo\\\/image\\\/\"}}]}<\/script>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"Serie de Seminarios Web sobre Uso de Normas Consensuadas Voluntarias - Regulatory Convergence","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/training-and-capacity-building-resources\/regulator-sessions\/serie-de-seminarios-web-sobre-uso-de-normas-consensuadas-voluntarias\/?lang=es","og_locale":"en_US","og_type":"article","og_title":"Serie de Seminarios Web sobre Uso de Normas Consensuadas Voluntarias - Regulatory Convergence","og_description":"El Proyecto de Convergencia Regulatoria de Dispositivos M\u00e9dicos co-liderado por USAID, ANSI, y AdvaMed a trav\u00e9s de la Coalici\u00f3n Interamericana para la Convergencia Regulatoria en el Sector de Tecnolog\u00eda M\u00e9dica, en colaboraci\u00f3n con la Administraci\u00f3n de Alimentos y Medicamentos de los Estados Unidos (USFDA) han organizado una serie de sesiones web sobre la utilizaci\u00f3n de Normas Internacionales con prop\u00f3sitos…","og_url":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/training-and-capacity-building-resources\/regulator-sessions\/serie-de-seminarios-web-sobre-uso-de-normas-consensuadas-voluntarias\/?lang=es","og_site_name":"Regulatory Convergence","article_modified_time":"2022-04-04T17:52:26+00:00","twitter_card":"summary_large_image","twitter_misc":{"Est. reading time":"4 minutes"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"WebPage","@id":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/training-and-capacity-building-resources\/regulator-sessions\/serie-de-seminarios-web-sobre-uso-de-normas-consensuadas-voluntarias\/?lang=es","url":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/training-and-capacity-building-resources\/regulator-sessions\/serie-de-seminarios-web-sobre-uso-de-normas-consensuadas-voluntarias\/?lang=es","name":"Serie de Seminarios Web sobre Uso de Normas Consensuadas Voluntarias - Regulatory Convergence","isPartOf":{"@id":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/?lang=es\/#website"},"datePublished":"2021-12-17T12:53:49+00:00","dateModified":"2022-04-04T17:52:26+00:00","breadcrumb":{"@id":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/training-and-capacity-building-resources\/regulator-sessions\/serie-de-seminarios-web-sobre-uso-de-normas-consensuadas-voluntarias\/?lang=es#breadcrumb"},"inLanguage":"en-US","potentialAction":[{"@type":"ReadAction","target":["https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/training-and-capacity-building-resources\/regulator-sessions\/serie-de-seminarios-web-sobre-uso-de-normas-consensuadas-voluntarias\/?lang=es"]}]},{"@type":"BreadcrumbList","@id":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/training-and-capacity-building-resources\/regulator-sessions\/serie-de-seminarios-web-sobre-uso-de-normas-consensuadas-voluntarias\/?lang=es#breadcrumb","itemListElement":[{"@type":"ListItem","position":1,"name":"Home","item":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/"},{"@type":"ListItem","position":2,"name":"Regulator Sessions","item":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/training-and-capacity-building-resources\/regulator-sessions\/"},{"@type":"ListItem","position":3,"name":"Serie de Seminarios Web sobre Uso de Normas Consensuadas Voluntarias"}]},{"@type":"WebSite","@id":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/?lang=es\/#website","url":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/?lang=es\/","name":"Regulatory Convergence","description":"Inter-American Coalition","publisher":{"@id":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/?lang=es\/#organization"},"potentialAction":[{"@type":"SearchAction","target":{"@type":"EntryPoint","urlTemplate":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/?lang=es\/?s={search_term_string}"},"query-input":{"@type":"PropertyValueSpecification","valueRequired":true,"valueName":"search_term_string"}}],"inLanguage":"en-US"},{"@type":"Organization","@id":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/?lang=es\/#organization","name":"Inter-American Coalition - Regulatory Convergence","url":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/?lang=es\/","logo":{"@type":"ImageObject","inLanguage":"en-US","@id":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/?lang=es\/#\/schema\/logo\/image\/","url":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/wp-content\/uploads\/sites\/4\/2021\/07\/logo_regulatory_retina_en.png","contentUrl":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/wp-content\/uploads\/sites\/4\/2021\/07\/logo_regulatory_retina_en.png","width":559,"height":280,"caption":"Inter-American Coalition - Regulatory Convergence"},"image":{"@id":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/?lang=es\/#\/schema\/logo\/image\/"}}]}},"uagb_featured_image_src":[],"uagb_author_info":{"display_name":"Guilherme Guain","author_link":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/author\/"},"uagb_comment_info":0,"uagb_excerpt":"El Proyecto de Convergencia Regulatoria de Dispositivos M\u00e9dicos co-liderado por USAID, ANSI, y AdvaMed a trav\u00e9s de la Coalici\u00f3n Interamericana para la Convergencia Regulatoria en el Sector de Tecnolog\u00eda M\u00e9dica, en colaboraci\u00f3n con la Administraci\u00f3n de Alimentos y Medicamentos de los Estados Unidos (USFDA) han organizado una serie de sesiones web sobre la utilizaci\u00f3n de Normas Internacionales con prop\u00f3sitos…","_links":{"self":[{"href":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/wp-json\/wp\/v2\/regulator-sessions\/3339","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/wp-json\/wp\/v2\/regulator-sessions"}],"about":[{"href":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/wp-json\/wp\/v2\/types\/regulator-sessions"}],"wp:attachment":[{"href":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/wp-json\/wp\/v2\/media?parent=3339"}],"wp:term":[{"taxonomy":"event_category","embeddable":true,"href":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/wp-json\/wp\/v2\/event_category?post=3339"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}