{"id":57123,"date":"2022-11-08T16:54:15","date_gmt":"2022-11-08T15:54:15","guid":{"rendered":"https:\/\/gxp-training.com\/online-course\/buenas-practicas-de-farmacovigilancia-gvp\/"},"modified":"2022-11-08T16:54:15","modified_gmt":"2022-11-08T15:54:15","slug":"buenas-practicas-de-farmacovigilancia-gvp","status":"publish","type":"product","link":"https:\/\/gxp-training.com\/es\/online-course\/buenas-practicas-de-farmacovigilancia-gvp\/","title":{"rendered":"Buenas Pr\u00e1cticas de Farmacovigilancia (GVP)"},"content":{"rendered":"<div class=\"description\">\n<p class=\"p1\">La Farmacovigilancia contribuye de manera esencial a la protecci\u00f3n de los pacientes y la salud p\u00fablica. Es altamente obligatorio para los fabricantes de ciencias de la vida seguir las GVP con programas que se centren en la evaluaci\u00f3n y gesti\u00f3n de riesgos. Este curso se basa en las directrices oficiales de GVP y es un programa de formaci\u00f3n completo para todas las personas que necesiten un repaso. Aprender\u00e1 sobre la identificaci\u00f3n y evaluaci\u00f3n de las se\u00f1ales de seguridad para una buena pr\u00e1ctica de notificaci\u00f3n, as\u00ed como las caracter\u00edsticas de un buen informe de caso. Al final, podr\u00e1 desarrollar un plan de farmacovigilancia.    <\/p>\n<p class=\"p1\">Este material fue elaborado por un equipo de Expertos en Asuntos Regulatorios con una cualificaci\u00f3n de la Northeastern University, Boston, pilotado por un Miembro Senior capaz de articular la teor\u00eda con la pr\u00e1ctica.<\/p>\n<\/div>\n<p>&nbsp;<\/p>\n<h3>Plan de estudios:<\/h3>\n<p>&nbsp;<\/p>\n<p><strong>Lecci\u00f3n 1: Identificaci\u00f3n de se\u00f1ales de seguridad<\/strong><\/p>\n<ul>\n<li>Caracter\u00edsticas de un buen informe de caso<\/li>\n<\/ul>\n<p><strong>Lecci\u00f3n 2: Investigaci\u00f3n de se\u00f1ales mediante estudios observacionales<\/strong><\/p>\n<ul>\n<li>Estudios farmacoepidemiol\u00f3gicos<\/li>\n<li>Registros<\/li>\n<li>Encuestas<\/li>\n<\/ul>\n<p><strong>Lecci\u00f3n 3: Interpretaci\u00f3n de se\u00f1ales de seguridad<\/strong><\/p>\n<ul>\n<li>Evaluaci\u00f3n de se\u00f1ales de seguridad<\/li>\n<\/ul>\n<p><strong>Lecci\u00f3n 4: C\u00f3mo desarrollar un plan de farmacovigilancia<\/strong><\/p>\n<ul>\n<li>Gu\u00eda de evaluaci\u00f3n farmacoepidemiol\u00f3gica<\/li>\n<li>Contenido de un plan de farmacovigilancia<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n<p><strong>Evaluaci\u00f3n<\/strong><\/p>\n","protected":false},"excerpt":{"rendered":"<p>La Farmacovigilancia contribuye de manera esencial a la protecci\u00f3n de los pacientes y la salud p\u00fablica. Es altamente obligatorio para los fabricantes de ciencias de la vida seguir las GVP con programas que se centren en la evaluaci\u00f3n y gesti\u00f3n de riesgos. Este curso se basa en las directrices oficiales de GVP y es un [&hellip;]<\/p>\n","protected":false},"featured_media":55797,"template":"","meta":{"_acf_changed":false,"content-type":""},"product_brand":[],"product_cat":[268,270,269],"product_tag":[],"class_list":{"0":"post-57123","1":"product","2":"type-product","3":"status-publish","4":"has-post-thumbnail","6":"product_cat-farmacovigilancia","7":"product_cat-organizacion-de-investigacion-por-contrato-cro","8":"product_cat-productos-farmaceuticos","10":"first","11":"instock","12":"taxable","13":"shipping-taxable","14":"purchasable","15":"product-type-subscription"},"bundled_by":[],"bundle_stock_status":"instock","bundle_stock_quantity":null,"bundle_virtual":false,"bundle_layout":"","bundle_add_to_cart_form_location":"","bundle_editable_in_cart":false,"bundle_sold_individually_context":"","bundle_item_grouping":"","bundle_min_size":"","bundle_max_size":"","bundle_price":[],"bundled_items":[],"bundle_sell_ids":[],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.5 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Buenas Pr\u00e1cticas de Farmacovigilancia (GVP) - Formaci\u00f3n Certificada y Acreditada<\/title>\n<meta name=\"description\" content=\"Aprenda Buenas Pr\u00e1cticas de Farmacovigilancia en l\u00ednea con los mejores expertos en asuntos regulatorios. 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