{"id":6342,"date":"2012-05-24T17:38:00","date_gmt":"2012-05-24T21:38:00","guid":{"rendered":"https:\/\/www.merkley.senate.gov\/merkley-applauds-passage-of-bill-to-speed-medical-innovations-to-market\/"},"modified":"2023-07-24T11:10:44","modified_gmt":"2023-07-24T15:10:44","slug":"merkley-applauds-passage-of-bill-to-speed-medical-innovations-to-market","status":"publish","type":"post","link":"https:\/\/www.merkley.senate.gov\/es\/merkley-applauds-passage-of-bill-to-speed-medical-innovations-to-market\/","title":{"rendered":"Merkley aplaude la aprobaci\u00f3n de un proyecto de ley para acelerar la comercializaci\u00f3n de innovaciones m\u00e9dicas"},"content":{"rendered":"

Washington, DC- Hoy, el Senado de los Estados Unidos aprob\u00f3 la Ley de Innovaci\u00f3n y Seguridad de la Administraci\u00f3n de Alimentos y Medicamentos (FDA), un proyecto de ley para brindarle a la FDA las herramientas necesarias para monitorear y revisar productos m\u00e9dicos y prevenir la escasez de medicamentos. El proyecto de ley inclu\u00eda dos disposiciones redactadas por el senador de Oreg\u00f3n, Jeff Merkley, para mejorar la seguridad de los dispositivos m\u00e9dicos.<\/p>\n

\n

"Los dispositivos m\u00e9dicos innovadores ayudan a salvar y mejorar la vida de los pacientes todos los d\u00edas", afirm\u00f3 Merkley. \u201cSin embargo, el fallo de los dispositivos m\u00e9dicos, en particular los que est\u00e1n implantados o son de soporte vital, puede provocar la muerte o una discapacidad y dolor significativos a largo plazo para los pacientes. Este proyecto de ley garantizar\u00e1 que los pacientes, los m\u00e9dicos y la FDA tengan la informaci\u00f3n y las herramientas que necesitan para mejorar la seguridad del paciente\u201d. <\/p>\n<\/blockquote>\n

Las disposiciones insertadas en el proyecto de ley por el senador Merkley reflejan fielmente la propuesta bipartidista. Ley de Garant\u00eda de Dispositivos M\u00e9dicos para Pacientes<\/a>, que el senador Merkley present\u00f3 en marzo. Requerir\u00e1 que la FDA implemente un sistema de Identificador \u00danico de Dispositivo para dispositivos implantables y de alto riesgo, de modo que, en caso de problemas de seguridad, los m\u00e9dicos y pacientes afectados puedan ser notificados. Las disposiciones de Merkley tambi\u00e9n agregan dispositivos m\u00e9dicos a la Iniciativa Sentinel, un sistema de datos electr\u00f3nico nacional integrado para rastrear los resultados de salud asociados con los medicamentos recetados. Esta base de datos permitir\u00e1 a la FDA detectar tendencias y se\u00f1alar posibles problemas de seguridad que los pacientes han experimentado con los dispositivos m\u00e9dicos.<\/p>\n

###<\/p>","protected":false},"excerpt":{"rendered":"

Washington, DC- Today, the United States Senate passed the Food and Drug Administration (FDA) Safety and Innovation Act, a bill to give the FDA the tools needed to monitor and review medical products and  prevent drug shortages. The bill included two provisions authored by Oregon’s Senator Jeff Merkley to improve the safety of medical devices. 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