{"id":57584,"date":"2023-10-31T07:55:23","date_gmt":"2023-10-31T07:55:23","guid":{"rendered":"https:\/\/gxp-training.com\/online-course\/cfr-part-210-et-211-cgmp-pour-les-produits-pharmaceutiques-finis\/"},"modified":"2023-10-31T07:55:23","modified_gmt":"2023-10-31T06:55:23","slug":"cfr-part-210-et-211-cgmp-pour-les-produits-pharmaceutiques-finis","status":"publish","type":"product","link":"https:\/\/gxp-training.com\/fr\/online-course\/cfr-part-210-et-211-cgmp-pour-les-produits-pharmaceutiques-finis\/","title":{"rendered":"CFR Part 210 et 211 : cGMP pour les produits pharmaceutiques finis"},"content":{"rendered":"<p>Plongez au c\u0153ur des nuances de la r\u00e9glementation de la fabrication pharmaceutique avec cette formation certifi\u00e9e en ligne, ax\u00e9e sur les CFR 210 &#038; 211 de la FDA. Comprenez les distinctions entre ces r\u00e9glementations car elles d\u00e9taillent divers aspects du <a href=\"https:\/\/gxp-training.com\/fr\/online-course\/introduction-aux-bonnes-pratiques-de-fabrication-bpf\/\">processus de fabrication pharmaceutique<\/a>. <\/p>\n<p><strong>Points forts du cours :<\/strong><\/p>\n<ul>\n<li>Analyse compl\u00e8te, des dispositions g\u00e9n\u00e9rales aux registres et rapports.<\/li>\n<li>Aper\u00e7u du contr\u00f4le des composants, de l\u2019emballage, de l\u2019\u00e9tiquetage et plus encore.<\/li>\n<li>Compr\u00e9hension pratique des r\u00e9glementations pour les responsables des op\u00e9rations et les responsables qualit\u00e9.<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n<p>Sous la direction du Dr Ciaran McEnister, un cadre pharmaceutique chevronn\u00e9 fort de plus de 25 ans d\u2019exp\u00e9rience en conformit\u00e9 r\u00e9glementaire, les apprenants b\u00e9n\u00e9ficient d\u2019une perspective compl\u00e8te. Le long parcours du Dr McEnister au sein d\u2019entreprises de premier plan garantit que ce cours est ancr\u00e9 dans une expertise concr\u00e8te. <\/p>\n<p>Ce cours convient \u00e0 toute personne travaillant dans la fabrication, les op\u00e9rations ou le contr\u00f4le qualit\u00e9 de produits pharmaceutiques commercialis\u00e9s ou distribu\u00e9s aux \u00c9tats-Unis (USA).<\/p>\n<p>Une fois la formation termin\u00e9e avec succ\u00e8s, les participants obtiennent un <a href=\"https:\/\/gxp-training.com\/fr\/certification-et-accreditation\/\">certificat de r\u00e9ussite<\/a> t\u00e9l\u00e9chargeable et tra\u00e7able que vous pouvez partager sur LinkedIn ou dans votre dossier RH personnel. Entamez d\u00e8s maintenant ce parcours r\u00e9glementaire \u00e0 votre rythme et renforcez votre expertise des exigences de la FDA am\u00e9ricaine pour les produits pharmaceutiques finis. <\/p>\n<p>&nbsp;<\/p>\n<h3>Programme :<\/h3>\n<p>&nbsp;<\/p>\n<p><strong>Aper\u00e7u du 21 CFR Part 210 &#038; 211<\/strong><\/p>\n<p><strong>Le\u00e7on 1 : Sous-partie A \u2013 Dispositions g\u00e9n\u00e9rales<\/strong><\/p>\n<p><strong>Le\u00e7on 2 : Sous-partie B \u2013 Organisation et personnel<\/strong><\/p>\n<p><strong>Le\u00e7on 3 : Sous-partie C \u2013 B\u00e2timents et installations<\/strong><\/p>\n<p><strong>Le\u00e7on 4 : Sous-partie D \u2013 \u00c9quipement<\/strong><\/p>\n<p><strong>Le\u00e7on 5 : Sous-partie E \u2013 Contr\u00f4le des composants, des r\u00e9cipients et des syst\u00e8mes de fermeture des m\u00e9dicaments<\/strong><\/p>\n<p><strong>Le\u00e7on 6 : Sous-partie F \u2013 Contr\u00f4les de la production et des processus<\/strong><\/p>\n<p><strong>Le\u00e7on 7 : Sous-partie G \u2013 Contr\u00f4le de l\u2019emballage et de l\u2019\u00e9tiquetage<\/strong><\/p>\n<p><strong>Le\u00e7on 8 : Sous-partie H \u2013 Stockage et distribution<\/strong><\/p>\n<p><strong>Le\u00e7on 9 : Sous-partie I \u2013 Contr\u00f4les en laboratoire<\/strong><\/p>\n<p><strong>Le\u00e7on 10 : Sous-partie J \u2013 Registres et rapports<\/strong><\/p>\n<p><strong>Le\u00e7on 11 : Sous-partie K \u2013 M\u00e9dicaments retourn\u00e9s et r\u00e9cup\u00e9r\u00e9s<\/strong><\/p>\n<p><strong>Conclusion<\/strong><\/p>\n<p><strong>\u00c9valuation<\/strong><\/p>\n<p><strong>Certification<\/strong><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Plongez au c\u0153ur des nuances de la r\u00e9glementation de la fabrication pharmaceutique avec cette formation certifi\u00e9e en ligne, ax\u00e9e sur les CFR 210 &#038; 211 de la FDA. Comprenez les distinctions entre ces r\u00e9glementations car elles d\u00e9taillent divers aspects du processus de fabrication pharmaceutique. Points forts du cours : Analyse compl\u00e8te, des dispositions g\u00e9n\u00e9rales aux [&hellip;]<\/p>\n","protected":false},"featured_media":44678,"template":"","meta":{"_acf_changed":false,"content-type":""},"product_brand":[],"product_cat":[257,254,258],"product_tag":[],"class_list":{"0":"post-57584","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-pharmaceutique","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>CFR PART 210 et 211 - Cours en ligne et certification<\/title>\n<meta name=\"description\" content=\"Inscrivez-vous d\u00e8s maintenant \u00e0 notre cours en ligne CFR PART 210 &amp; 211. 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