{"id":3279,"date":"2021-12-01T17:37:09","date_gmt":"2021-12-01T17:37:09","guid":{"rendered":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/training-and-capacity-building-resources\/policy-training\/serie-de-webinarios-sobre-buenas-practicas-regulatorias-y-su-implementacion-en-el-sector-de-dispositivos-medicos-en-mexico\/"},"modified":"2022-02-23T11:52:30","modified_gmt":"2022-02-23T11:52:30","slug":"serie-de-webinarios-sobre-buenas-practicas-regulatorias-y-su-implementacion-en-el-sector-de-dispositivos-medicos-en-mexico","status":"publish","type":"policy-training","link":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/training-and-capacity-building-resources\/policy-training\/serie-de-webinarios-sobre-buenas-practicas-regulatorias-y-su-implementacion-en-el-sector-de-dispositivos-medicos-en-mexico\/?lang=es","title":{"rendered":"Serie de Webinarios sobre Buenas Pr\u00e1cticas Regulatorias y su Implementaci\u00f3n en el Sector de Dispositivos M\u00e9dicos en M\u00e9xico"},"content":{"rendered":"\n

La Coalici\u00f3n Interamericana para la Convergencia Regulatoria en el Sector de Tecnolog\u00eda M\u00e9dica, en el marco del Proyecto de Convergencia Regulatoria de Dispositivos M\u00e9dicos (MDRC) de la Alianza por las Normas, en el que participan USAID, ANSI y AdvaMed, en colaboraci\u00f3n con la Comisi\u00f3n Federal para la Protecci\u00f3n contra Riesgos Sanitarios (COFEPRIS), organizaron esta Serie sobre Buenas Pr\u00e1cticas Regulatorias y su Implementaci\u00f3n en el Sector de Dispositivos M\u00e9dicos, que se llevaron a cabo los d\u00edas 27 de octubre, 10, 17 y 24 de noviembre del 2021.<\/p>\n\n\n\n

La capacitaci\u00f3n tuvo por objeto promover, mediante el intercambio de experiencias, la utilizaci\u00f3n de Buenas Practicas Regulatorias en el proceso de implementaci\u00f3n de normas internacionales para fines regulatorios de Dispositivos M\u00e9dicos. El evento se present\u00f3 como un seminario virtual que const\u00f3 de cuatro sesiones queincluyeron generalidades y compromisos internacionales, las Buenas Pr\u00e1cticas Regulatorias en el \u00e1mbito internacional y nacional de los dispositivos m\u00e9dicos, procesos reglamentarios en M\u00e9xico y desaf\u00edos y oportunidades de la convergencia regulatoria en el sector de los dispositivos m\u00e9dicos.<\/p>\n\n\n\n

Sesi\u00f3n I<\/h2>\n\n\n\n

Agenda<\/h3>\n\n\n\n
\n
Espa\u00f1ol<\/a><\/div>\n<\/div>\n\n\n\n

Grabaci\u00f3n<\/h3>\n\n\n\n
\n
Espa\u00f1ol<\/a><\/div>\n<\/div>\n\n\n\n

Presentaciones<\/h3>\n\n\n\n
\n
<\/a>
<\/path><\/svg><\/span><\/span>
Introducci\u00f3n y Panorama General de las Buenas Pr\u00e1cticas Regulatorias, Renata Amaral, IACRC<\/span><\/div><\/div><\/div>\n\n\n\n
<\/a>
<\/path><\/svg><\/span><\/span>
Diagn\u00f3stico y Sensibilizaci\u00f3n acerca de los Acuerdos Comerciales Internacionales, Ricardo Aranda, Dorantes Advisors<\/span><\/div><\/div><\/div>\n\n\n\n
<\/a>
<\/path><\/svg><\/span><\/span>
La Observancia de las Obligaciones Internacionales, N. Viviana Salgado, Secretar\u00eda de Econom\u00eda<\/span><\/div><\/div><\/div>\n\n\n\n
<\/a>
<\/path><\/svg><\/span><\/span>
La Observancia de las Obligaciones Internacionales, Juan A. Dorantes, Dorantes Advisors<\/span><\/div><\/div><\/div>\n<\/div><\/div>\n\n\n\n

Sesi\u00f3n II<\/h2>\n\n\n\n

Agenda <\/h3>\n\n\n\n
\n
Espa\u00f1ol<\/a><\/div>\n<\/div>\n\n\n\n

Grabaci\u00f3n<\/h3>\n\n\n\n
\n
Espa\u00f1ol<\/a><\/div>\n<\/div>\n\n\n\n

Presentaciones<\/h3>\n\n\n\n
\n
<\/a>
<\/path><\/svg><\/span><\/span>
Buenas pr\u00e1cticas regulatorias en la regulaci\u00f3n de productos m\u00e9dicos, Agnes S. Kijo, OMS<\/span><\/div><\/div><\/div>\n\n\n\n
<\/a>
<\/path><\/svg><\/span><\/span>
Ley de Infraestructura de Calidad \u2013 Juan Carlos Rivera, DGN<\/span><\/div><\/div><\/div>\n\n\n\n
<\/a>
<\/path><\/svg><\/span><\/span>
Estado de la Implementaci\u00f3n de las Buenas Pr\u00e1cticas Regulatorias \u2013 Helga Castillo, COFEPRIS<\/span><\/div><\/div><\/div>\n<\/div><\/div>\n\n\n\n

Sesi\u00f3n III<\/h2>\n\n\n\n

Agenda <\/h3>\n\n\n\n
\n
Espa\u00f1ol<\/a><\/div>\n<\/div>\n\n\n\n

Grabaci\u00f3n<\/h3>\n\n\n\n
\n
Espa\u00f1ol<\/a><\/div>\n<\/div>\n\n\n\n

Presentaciones<\/h3>\n\n\n\n

El Proceso de desarrollo de Reglamentos T\u00e9cnicos aplicables a los Dispositivos M\u00e9dicos y Reactivos de Diagn\u00f3stico in vitro y la garant\u00eda de cumplimiento de obligaciones internacionales:<\/h4>\n\n\n\n

Parte I<\/h5>\n\n\n\n
\n
<\/a>
<\/path><\/svg><\/span><\/span>
Regulaci\u00f3n de Insumos para la Salud – Jonathan R. Flores, CAS, COFEPRIS<\/span><\/div><\/div><\/div>\n\n\n\n
<\/a>
<\/path><\/svg><\/span><\/span>
Normas Oficiales Mexicanas \u2013 Victor Torres, DGN<\/span><\/div><\/div><\/div>\n<\/div><\/div>\n\n\n\n
Parte II<\/h5>\n\n\n\n
\n
<\/a>
<\/path><\/svg><\/span><\/span>
El Proceso Regulatorio en la COFEPRIS, An\u00e1lisis de Impacto Regulatorio, Consultas P\u00fablicas, Notificaciones OTC, Berenice Terrazas, CGJC, COFEPRIS<\/span><\/div><\/div><\/div>\n\n\n\n
<\/a>
<\/path><\/svg><\/span><\/span>
Farmacopea de los Estados Unidos Mexicanos \u2013 Suplemento de Dispositivos M\u00e9dicos. Rafael Hern\u00e1ndez, FEUM.<\/span><\/div><\/div><\/div>\n<\/div><\/div>\n\n\n\n

Sesi\u00f3n IV<\/h2>\n\n\n\n

Agenda<\/h3>\n\n\n\n
\n
Espa\u00f1ol<\/a><\/div>\n<\/div>\n\n\n\n

Grabaci\u00f3n<\/h3>\n\n\n\n
\n
Espa\u00f1ol<\/a><\/div>\n<\/div>\n\n\n\n

Semblanza de los Panelistas<\/h3>\n\n\n\n
\n
Espa\u00f1ol<\/a><\/div>\n<\/div>\n\n\n\n

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