{"id":15983,"date":"2024-12-31T13:34:00","date_gmt":"2024-12-31T16:34:00","guid":{"rendered":"https:\/\/allende.com\/?p=15983"},"modified":"2024-12-31T13:35:19","modified_gmt":"2024-12-31T16:35:19","slug":"new-regulation-by-anmat-on-procedures-for-the-inspection-of-manufacturers-of-medical-devices-and-in-vitro-diagnostic-products","status":"publish","type":"post","link":"https:\/\/allende.com\/en\/life-sciences-en\/new-regulation-by-anmat-on-procedures-for-the-inspection-of-manufacturers-of-medical-devices-and-in-vitro-diagnostic-products-12-31-2024\/","title":{"rendered":"New Regulation by ANMAT on Procedures for the Inspection of Manufacturers of Medical Devices and In Vitro Diagnostic Products"},"content":{"rendered":"<p>Through Disposition No. 11419\/2024, the National Administration of Drugs, Food, and Medical Technology (ANMAT) incorporated into the national legal framework the Mercosur Common Market Group (GMC) Resolution No. 20\/17 concerning procedures for the inspection of manufacturers of Medical Devices and <em>In Vitro<\/em> Diagnostic Products, along with its amendments introduced by GMC Resolution N\u00b034\/23.<\/p>\n<p>GMC Resolution No. 20\/17 updated the common procedures for conducting health inspections of manufacturers of Medical Devices and <em>In Vitro<\/em> Diagnostic Products, based on the experience gained through joint actions within the Mercosur framework.<\/p>\n<p>Consequently, with the incorporation of these Resolutions, ANMAT Disposition No. 3265\/13, which had incorporated the earlier Mercosur GMC Resolution No. 32\/12 on common procedures for inspecting manufacturers of Medical Devices and In Vitro Diagnostic Products in the Member States, was repealed.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Through Disposition No. 11419\/2024, the National Administration of Drugs, Food, and Medical Technology (ANMAT) incorporated into the national legal framework the Mercosur Common Market Group (GMC) Resolution No. 20\/17 concerning procedures for the inspection of manufacturers of Medical Devices and In Vitro Diagnostic Products, along with its amendments introduced by GMC Resolution N\u00b034\/23. GMC Resolution [&hellip;]<\/p>\n","protected":false},"author":11,"featured_media":15981,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"_eb_attr":"","footnotes":""},"categories":[53],"tags":[],"class_list":["post-15983","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-life-sciences-en"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.4 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>New Regulation by ANMAT on Procedures for the Inspection of Manufacturers of Medical Devices and In Vitro Diagnostic Products - Allende &amp; Brea - Estudio Jur\u00eddico<\/title>\n<meta name=\"description\" content=\"Through Disposition No. 11419\/2024, the National Administration of Drugs, Food, and Medical Technology (ANMAT) incorporated into the national legal\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/allende.com\/en\/life-sciences-en\/new-regulation-by-anmat-on-procedures-for-the-inspection-of-manufacturers-of-medical-devices-and-in-vitro-diagnostic-products-12-31-2024\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"New Regulation by ANMAT on Procedures for the Inspection of Manufacturers of Medical Devices and In Vitro Diagnostic Products - 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