{"id":57749,"date":"2022-12-09T15:42:12","date_gmt":"2022-12-09T15:42:12","guid":{"rendered":"https:\/\/gxp-training.com\/online-course\/buenas-practicas-de-documentacion-gdocp\/"},"modified":"2022-12-09T15:42:12","modified_gmt":"2022-12-09T14:42:12","slug":"buenas-practicas-de-documentacion-gdocp","status":"publish","type":"product","link":"https:\/\/gxp-training.com\/es\/online-course\/buenas-practicas-de-documentacion-gdocp\/","title":{"rendered":"Buenas Pr\u00e1cticas de Documentaci\u00f3n (GDocP)"},"content":{"rendered":"<p>Los errores de documentaci\u00f3n se encuentran entre los hallazgos m\u00e1s comunes en las inspecciones de <a href=\"https:\/\/gxp-training.com\/es\/gxp-courses\/bpf-buenas-practicas-de-fabricacion\/\">GMP<\/a> y entre los m\u00e1s prevenibles. Este curso abarca las <a href=\"https:\/\/www.fda.gov\/media\/185615\/download\">Buenas Pr\u00e1cticas de Documentaci\u00f3n<\/a> (GDocP) en las que conf\u00edan las organizaciones reguladas para mantener los registros precisos, conformes y listos para auditor\u00eda en fabricaci\u00f3n, ensayos y operaciones de calidad. <\/p>\n<p><strong>\u00bfQu\u00e9 aprender\u00e1?<\/strong><\/p>\n<ul>\n<li>Principios de las <a href=\"https:\/\/www.fda.gov\/media\/185615\/download\">Buenas Pr\u00e1cticas de Documentaci\u00f3n<\/a> en GMP<\/li>\n<li>C\u00f3mo completar, revisar y mantener distintos documentos GMP<\/li>\n<li>Identificar y corregir errores de documentaci\u00f3n habituales<\/li>\n<li>Garantizar el cumplimiento mediante un control y una conservaci\u00f3n adecuados de los documentos<\/li>\n<\/ul>\n<p><strong>\u00bfQui\u00e9n deber\u00eda inscribirse?<\/strong><\/p>\n<ul>\n<li>Profesionales de aseguramiento y control de calidad<\/li>\n<li><a href=\"https:\/\/gxp-training.com\/online-course\/regulatory-affairs-specialist-training-certification\/\">Especialistas en asuntos regulatorios<\/a><\/li>\n<li>Personal de fabricaci\u00f3n y laboratorio que gestiona documentaci\u00f3n<\/li>\n<li><a href=\"https:\/\/gxp-training.com\/es\/online-course\/auditoria-gmp-interna-rol-del-auditor-gmp\/\">Auditores internos<\/a> y equipos de cumplimiento<\/li>\n<\/ul>\n<p>Tras completar el curso con \u00e9xito, recibir\u00e1 un <strong>certificado validado acreditado con cr\u00e9ditos CPD\/CEU<\/strong>, adecuado para documentaci\u00f3n de auditor\u00eda y cumplimiento.<\/p>\n<h3>Programa:<\/h3>\n<p><strong>Introducci\u00f3n<\/strong><\/p>\n<p><strong>Cap\u00edtulo 1: \u00bfQu\u00e9 son las Buenas Pr\u00e1cticas de Documentaci\u00f3n?<\/strong><\/p>\n<p><strong>Cap\u00edtulo 2: C\u00f3mo y cu\u00e1ndo aplicar las Buenas Pr\u00e1cticas de Documentaci\u00f3n<\/strong><\/p>\n<p><strong>Cap\u00edtulo 3: Tipos de documentos<\/strong><\/p>\n<ul dir=\"ltr\">\n<li>Documentos de compromiso (p. ej., solicitudes de nuevo medicamento, nuevos expedientes maestros de medicamento)<\/li>\n<li>Documentos directivos (p. ej., especificaciones, STP, SOP, MPR)<\/li>\n<li>Documentos de registro (p. ej., protocolos, BPR, libros de registro, registros de calibraci\u00f3n)<\/li>\n<\/ul>\n<p><strong>Cap\u00edtulo 4: Normas de buena documentaci\u00f3n<\/strong><\/p>\n<ul dir=\"ltr\">\n<li>Aprobaci\u00f3n<\/li>\n<li>Claridad<\/li>\n<li>Revisi\u00f3n y actualizaci\u00f3n peri\u00f3dicas<\/li>\n<li>Presentaci\u00f3n formal<\/li>\n<li>Registros<\/li>\n<\/ul>\n<p><strong>Cap\u00edtulo 5: C\u00f3mo completar la documentaci\u00f3n, incluidos los formularios de recogida de datos y los registros de lote<\/strong><\/p>\n<p><strong>Cap\u00edtulo 6: C\u00f3mo a\u00f1adir datos brutos a formularios y cuadernos de laboratorio<\/strong><\/p>\n<p><strong>Cap\u00edtulo 7: Errores t\u00edpicos<\/strong><\/p>\n<p><strong>Cap\u00edtulo 8: C\u00f3mo corregir errores y omisiones en la introducci\u00f3n de datos<\/strong><\/p>\n<p><strong>Cap\u00edtulo 9: C\u00f3mo fechar, firmar y marcar los registros<\/strong><\/p>\n<p><strong>Evaluaci\u00f3n<\/strong><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Los errores de documentaci\u00f3n se encuentran entre los hallazgos m\u00e1s comunes en las inspecciones de GMP y entre los m\u00e1s prevenibles. Este curso abarca las Buenas Pr\u00e1cticas de Documentaci\u00f3n (GDocP) en las que conf\u00edan las organizaciones reguladas para mantener los registros precisos, conformes y listos para auditor\u00eda en fabricaci\u00f3n, ensayos y operaciones de calidad. \u00bfQu\u00e9 [&hellip;]<\/p>\n","protected":false},"featured_media":55217,"template":"","meta":{"_acf_changed":false,"content-type":""},"product_brand":[],"product_cat":[280,265,271,275,278,273,272,270,269,266],"product_tag":[],"class_list":{"0":"post-57749","1":"product","2":"type-product","3":"status-publish","4":"has-post-thumbnail","6":"product_cat-bpd-buenas-practicas-de-distribucion","7":"product_cat-bpf-buenas-practicas-de-fabricacion","8":"product_cat-garantia-de-calidad","9":"product_cat-gcp-ensayos-clinicos","10":"product_cat-glp-buenas-practicas-de-laboratorio","11":"product_cat-intersectorial","12":"product_cat-laboratorios","13":"product_cat-organizacion-de-investigacion-por-contrato-cro","14":"product_cat-productos-farmaceuticos","15":"product_cat-productos-sanitarios","17":"first","18":"instock","19":"taxable","20":"shipping-taxable","21":"purchasable","22":"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 Documentaci\u00f3n (GDocP): Curso online certificado<\/title>\n<meta name=\"description\" content=\"Buenas Pr\u00e1cticas de Documentaci\u00f3n (GDocP). 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