{"id":419,"date":"2024-01-24T13:54:39","date_gmt":"2024-01-24T12:54:39","guid":{"rendered":"https:\/\/www.asinfarma.com\/seminario-expertos\/?p=419"},"modified":"2025-12-30T10:20:40","modified_gmt":"2025-12-30T09:20:40","slug":"retos-asociados-a-la-implementacion-del-pupsit","status":"publish","type":"post","link":"https:\/\/www.asinfarma.com\/seminario-expertos\/2024\/retos-asociados-a-la-implementacion-del-pupsit\/","title":{"rendered":"Retos asociados a la implementaci\u00f3n del PUPSIT"},"content":{"rendered":"\n<div class=\"wp-block-columns is-layout-flex wp-container-core-columns-is-layout-9d6595d7 wp-block-columns-is-layout-flex\">\n<div class=\"wp-block-column is-layout-flow wp-block-column-is-layout-flow\">\n<p><strong>Ponentes<\/strong>: <\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li><em>Dra. Gloria Pontes, CYTIVA SPAIN<\/em><\/li>\n\n\n\n<li><em>Raquel Llobell, CYTIVA SPAIN<\/em><\/li>\n<\/ul>\n\n\n\n<p>Con la nueva revisi\u00f3n del Anexo 1 de EU GMP, el panorama para la fabricaci\u00f3n de medicamentos est\u00e9riles est\u00e1 evolucionando. Las pruebas de integridad previas al uso y posteriores a la esterilizaci\u00f3n o PUPSIT, aunque no son un requisito regulatorio nuevo, plantean nuevos desaf\u00edos para los usuarios:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Desaf\u00edos en la implementaci\u00f3n del PUPSIT<\/li>\n\n\n\n<li>Estrategias sobre c\u00f3mo realizar el PUPSIT de manera segura<\/li>\n<\/ul>\n<\/div>\n\n\n\n<div class=\"wp-block-column is-layout-flow wp-block-column-is-layout-flow\">\n<div id=\"GloriaPontes\" class=\"wp-block-group round has-global-color-13-background-color has-background\"><div class=\"wp-block-group__inner-container is-layout-flow wp-block-group-is-layout-flow\"><div class=\"wp-block-image is-style-rounded\">\n<figure class=\"aligncenter size-thumbnail is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"150\" height=\"150\" src=\"https:\/\/www.asinfarma.com\/seminario-expertos\/wp-content\/uploads\/sites\/2\/2024\/01\/Gloria-Pontes-150x150.jpg\" alt=\"Gloria Pontes\" class=\"wp-image-274\" style=\"width:200px\" srcset=\"https:\/\/www.asinfarma.com\/seminario-expertos\/wp-content\/uploads\/sites\/2\/2024\/01\/Gloria-Pontes-150x150.jpg 150w, https:\/\/www.asinfarma.com\/seminario-expertos\/wp-content\/uploads\/sites\/2\/2024\/01\/Gloria-Pontes.jpg 200w\" sizes=\"auto, (max-width: 150px) 100vw, 150px\" \/><\/figure><\/div>\n\n\n<div style=\"height:20px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<p class=\"has-text-align-center\"><strong>Dra. Gloria Pontes<\/strong><\/p>\n\n\n\n<p class=\"has-text-align-center\" style=\"font-size:15px\"><strong>Scientist II Field Team Manager <\/strong><br>Cytiva Spain SLU  <\/p>\n\n\n<div style=\"font-size:15px\"><div class=\"su-expand su-expand-collapsed su-expand-link-style-underlined\" data-height=\"1\"><div class=\"su-expand-content su-u-trim\" style=\"color:#333333;max-height:1px;overflow:hidden\">\n\n\n\n<p style=\"font-size:15px\">Graduada en Ingenier\u00eda Biom\u00e9dica y Doctora en Ingenier\u00eda de Materiales con especializaci\u00f3n en Biomateriales. 5 a\u00f1os de experiencia en investigaci\u00f3n y 2 a\u00f1os dando soporte t\u00e9cnico en el sector farmac\u00e9utico.<\/p>\n\n\n<\/div><div class=\"su-expand-link su-expand-link-more\" style=\"text-align:center\"><a href=\"javascript:;\" style=\"color:#176585;border-color:#176585\"><i class=\"sui sui-plus\" style=\"\" aria-label=\"\"><\/i><span style=\"border-color:#176585\">Ver m\u00e1s<\/span><\/a><\/div><div class=\"su-expand-link su-expand-link-less\" style=\"text-align:center\"><a href=\"javascript:;\" style=\"color:#176585;border-color:#176585\"><i class=\"sui sui-minus\" style=\"\" aria-label=\"\"><\/i><span style=\"border-color:#176585\">Ver menos<\/span><\/a><\/div><\/div><\/div>\n\n\n\n<p> <\/p>\n<\/div><\/div>\n\n\n\n<div style=\"height:20px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n<\/div>\n\n\n\n<div class=\"wp-block-column is-layout-flow wp-block-column-is-layout-flow\">\n<div id=\"RaquelLlobell\" class=\"wp-block-group round has-global-color-13-background-color has-background\"><div class=\"wp-block-group__inner-container is-layout-flow wp-block-group-is-layout-flow\"><div class=\"wp-block-image is-style-rounded\">\n<figure class=\"aligncenter size-thumbnail is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"150\" height=\"150\" src=\"https:\/\/www.asinfarma.com\/seminario-expertos\/wp-content\/uploads\/sites\/2\/2024\/01\/Raquel-Llobell-150x150.jpg\" alt=\"Raquel Llobell\" class=\"wp-image-277\" style=\"width:200px\" srcset=\"https:\/\/www.asinfarma.com\/seminario-expertos\/wp-content\/uploads\/sites\/2\/2024\/01\/Raquel-Llobell-150x150.jpg 150w, https:\/\/www.asinfarma.com\/seminario-expertos\/wp-content\/uploads\/sites\/2\/2024\/01\/Raquel-Llobell.jpg 200w\" sizes=\"auto, (max-width: 150px) 100vw, 150px\" \/><\/figure><\/div>\n\n\n<div style=\"height:20px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<p class=\"has-text-align-center\"><strong>Raquel Llobell<\/strong><\/p>\n\n\n\n<p class=\"has-text-align-center\" style=\"font-size:15px\"><strong>Account Manager Bioprocess Biopharma <\/strong><br>Cytiva Spain SLU <\/p>\n\n\n<div style=\"font-size:15px\"><div class=\"su-expand su-expand-collapsed su-expand-link-style-underlined\" data-height=\"1\"><div class=\"su-expand-content su-u-trim\" style=\"color:#333333;max-height:1px;overflow:hidden\">\n\n\n\n<p style=\"font-size:15px\">Licenciada en Farmacia especialista en Farmacia Industrial y Gal\u00e9nica. 36 a\u00f1os colaborando, asesorando y buscando soluciones en el sector farmac\u00e9utico desde diferentes posiciones en Pall Espa\u00f1a y actualmente en Cytiva Spain.<\/p>\n\n\n<\/div><div class=\"su-expand-link su-expand-link-more\" style=\"text-align:center\"><a href=\"javascript:;\" style=\"color:#176585;border-color:#176585\"><i class=\"sui sui-plus\" style=\"\" aria-label=\"\"><\/i><span style=\"border-color:#176585\">Ver m\u00e1s<\/span><\/a><\/div><div class=\"su-expand-link su-expand-link-less\" style=\"text-align:center\"><a href=\"javascript:;\" style=\"color:#176585;border-color:#176585\"><i class=\"sui sui-minus\" style=\"\" aria-label=\"\"><\/i><span style=\"border-color:#176585\">Ver menos<\/span><\/a><\/div><\/div><\/div>\n\n\n\n<p> <\/p>\n<\/div><\/div>\n\n\n\n<div style=\"height:20px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<figure class=\"wp-block-image size-large\"><img decoding=\"async\" src=\"https:\/\/www.asinfarma.com\/seminario-expertos\/wp-content\/uploads\/sites\/2\/2024\/01\/logo-seminario-expertos.svg\" alt=\"Seminario expertos en procesos as\u00e9pticos\" class=\"wp-image-164\"\/><\/figure>\n<\/div>\n<\/div>\n","protected":false},"excerpt":{"rendered":"<p>Ponentes: Con la nueva revisi\u00f3n del Anexo 1 de EU GMP, el panorama para la fabricaci\u00f3n de medicamentos est\u00e9riles est\u00e1 evolucionando. Las pruebas de integridad previas al uso y posteriores a la esterilizaci\u00f3n o PUPSIT, aunque no son un requisito regulatorio nuevo, plantean nuevos desaf\u00edos para los usuarios: Dra. Gloria Pontes Scientist II Field Team &#8230; <a title=\"Retos asociados a la implementaci\u00f3n del PUPSIT\" class=\"read-more\" href=\"https:\/\/www.asinfarma.com\/seminario-expertos\/2024\/retos-asociados-a-la-implementacion-del-pupsit\/\" aria-label=\"Leer m\u00e1s sobre Retos asociados a la implementaci\u00f3n del PUPSIT\">Leer m\u00e1s<\/a><\/p>\n","protected":false},"author":3,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"inline_featured_image":false,"footnotes":""},"categories":[1],"tags":[9],"class_list":["post-419","post","type-post","status-publish","format-standard","hentry","category-sin-categoria","tag-9","generate-columns","tablet-grid-50","mobile-grid-100","grid-parent","grid-50"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.6 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Retos asociados a la implementaci\u00f3n del PUPSIT - Seminario de 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