{"id":57174,"date":"2022-05-27T11:56:00","date_gmt":"2022-05-27T09:56:00","guid":{"rendered":"https:\/\/gxp-training.com\/online-course\/enregistrements-archivage-et-conservation\/"},"modified":"2022-05-27T11:56:00","modified_gmt":"2022-05-27T09:56:00","slug":"enregistrements-archivage-et-conservation","status":"publish","type":"product","link":"https:\/\/gxp-training.com\/fr\/online-course\/enregistrements-archivage-et-conservation\/","title":{"rendered":"Enregistrements, Archivage et Conservation"},"content":{"rendered":"<p>On peut difficilement pr\u00e9tendre avoir \u00e9t\u00e9 form\u00e9 \u00e0 la fabrication pharmaceutique sans avoir entendu l\u2019adage \u00ab si ce n\u2019est pas document\u00e9, cela n\u2019a jamais eu lieu \u00bb. Cela souligne l\u2019importance de la documentation dans le processus de fabrication. C\u2019est l\u2019objet de ce cours.  <\/p>\n<p>Les participants apprendront comment les informations document\u00e9es sont g\u00e9r\u00e9es en fonction de leur pertinence et de leur anciennet\u00e9 (archivage et conservation). Vous d\u00e9couvrirez \u00e9galement comment ces informations peuvent \u00eatre exploit\u00e9es pour de futures modifications du processus de production. <\/p>\n<p>&nbsp;<\/p>\n<p>Dans ce cours, nous proposons une synth\u00e8se du sujet \u00e0 travers une exp\u00e9rience interactive en ligne. Ce mat\u00e9riel a \u00e9t\u00e9 \u00e9labor\u00e9 par une \u00e9quipe d\u2019experts en affaires r\u00e9glementaires, dipl\u00f4m\u00e9s de la Northeastern University, Boston, et pilot\u00e9 par un membre senior capable d\u2019articuler la th\u00e9orie et la pratique. <\/p>\n<p>&nbsp;<\/p>\n<h3>Programme<\/h3>\n<p>&nbsp;<\/p>\n<p><strong>Introduction<\/strong><\/p>\n<p>&nbsp;<\/p>\n<p><strong>Le\u00e7on 1 : Quelles sont les bonnes pratiques de gestion des donn\u00e9es et des enregistrements ?<\/strong><\/p>\n<p>&nbsp;<\/p>\n<ul>\n<li>N\u00e9cessit\u00e9 de bonnes pratiques de gestion des donn\u00e9es et des enregistrements<\/li>\n<li>Ce qui rel\u00e8ve des bonnes pratiques de gestion des donn\u00e9es et des enregistrements<\/li>\n<li>Qui est responsable des bonnes pratiques de gestion des donn\u00e9es et des enregistrements ?<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n<p><strong>Le\u00e7on 2 : Mise en \u0153uvre des bonnes pratiques de gestion des donn\u00e9es et des enregistrements en GxP<\/strong><\/p>\n<p>&nbsp;<\/p>\n<p><strong>Le\u00e7on 3 : Cycle de vie d\u2019un enregistrement<\/strong><\/p>\n<p>&nbsp;<\/p>\n<ul>\n<li>Collecte et enregistrement des donn\u00e9es<\/li>\n<li>Traitement des donn\u00e9es<\/li>\n<li>Examen et rapport des donn\u00e9es<\/li>\n<li>Conservation et r\u00e9cup\u00e9ration des donn\u00e9es<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n<p><strong>Le\u00e7on 4 : Organisation du syst\u00e8me d\u2019enregistrements dans une configuration GxP<\/strong><\/p>\n<p>&nbsp;<\/p>\n<ul>\n<li>Syst\u00e8me documentaire hi\u00e9rarchique<\/li>\n<li>Niveau 1 \u2013 Manuel Qualit\u00e9<\/li>\n<li>Niveau 2 \u2013 Politiques de l\u2019entreprise<\/li>\n<li>Niveau 3 \u2013 Proc\u00e9dures Op\u00e9ratoires Standard (POS)<\/li>\n<li>Niveau 4 \u2013 Dossiers de lots, m\u00e9thodes d\u2019essai, sp\u00e9cifications, documents de validation<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n<p><strong>Le\u00e7on 5 : Document ma\u00eetre d\u2019une configuration GxP : Fichier Ma\u00eetre du Site<\/strong><\/p>\n<p>&nbsp;<\/p>\n<ul>\n<li>Composants d\u2019un Fichier Ma\u00eetre du Site<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n<p><strong>Le\u00e7on 6 : Liste des documents courants conserv\u00e9s dans une configuration GxP<\/strong><\/p>\n<p>&nbsp;<\/p>\n<ul>\n<li>Informations requises dans les documents selon le RGPD<\/li>\n<li>Document 1 : Sp\u00e9cifications<\/li>\n<li>Document 2 : Formule de fabrication et instructions de traitement<\/li>\n<li>Document 3 : Instructions d\u2019emballage<\/li>\n<li>Document 4 : Dossiers de traitement des lots<\/li>\n<li>Document 5 : Dossiers d\u2019emballage des lots<\/li>\n<li>Document 6 : R\u00e9ception<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n<p><strong>Le\u00e7on 7 : Enregistrements, Archivage et Conservation selon les principes du RGPD dans une configuration GxP<\/strong><\/p>\n<p>&nbsp;<\/p>\n<ul>\n<li>Points cl\u00e9s pour les enregistrements<\/li>\n<li>Validation des enregistrements \u00e9lectroniques<\/li>\n<li>Maintenance, conservation et archivage des enregistrements<\/li>\n<\/ul>\n<p><strong> <\/strong><\/p>\n<p><strong>Glossaire<\/strong><\/p>\n<p>&nbsp;<\/p>\n<p><strong>Conclusion<\/strong><\/p>\n<p>&nbsp;<\/p>\n<p><strong>Quiz<\/strong><\/p>\n","protected":false},"excerpt":{"rendered":"<p>On peut difficilement pr\u00e9tendre avoir \u00e9t\u00e9 form\u00e9 \u00e0 la fabrication pharmaceutique sans avoir entendu l\u2019adage \u00ab si ce n\u2019est pas document\u00e9, cela n\u2019a jamais eu lieu \u00bb. Cela souligne l\u2019importance de la documentation dans le processus de fabrication. C\u2019est l\u2019objet de ce cours. Les participants apprendront comment les informations document\u00e9es sont g\u00e9r\u00e9es en fonction de [&hellip;]<\/p>\n","protected":false},"featured_media":43776,"template":"","meta":{"_acf_changed":false,"content-type":""},"product_brand":[],"product_cat":[257,254,263,258],"product_tag":[],"class_list":{"0":"post-57174","1":"product","2":"type-product","3":"status-publish","4":"has-post-thumbnail","6":"product_cat-assurance-qualite","7":"product_cat-bpf-bonnes-pratiques-de-fabrication","8":"product_cat-organisme-de-recherche-sous-contrat-cro","9":"product_cat-pharmaceutique","11":"first","12":"instock","13":"taxable","14":"shipping-taxable","15":"purchasable","16":"product-type-simple"},"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>Enregistrements, Archivage et Conservation \u2013 Formations GxP Certifi\u00e9es en Ligne<\/title>\n<meta name=\"description\" content=\"La documentation permet de r\u00e9examiner les processus pour diverses raisons. 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