{"id":4145,"date":"2022-05-31T20:46:35","date_gmt":"2022-05-31T20:46:35","guid":{"rendered":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/?page_id=4145"},"modified":"2022-06-02T10:46:01","modified_gmt":"2022-06-02T10:46:01","slug":"mexico","status":"publish","type":"page","link":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/coalition-action\/positions\/mexico\/","title":{"rendered":"Mexico"},"content":{"rendered":"\n<div class=\"wp-block-uagb-info-box mb-1 uagb-infobox__outer-wrap uagb-block-2e7d8930\"><div class=\"uagb-infobox__content-wrap uagb-infobox uagb-infobox-has-image uagb-infobox-icon-left uagb-infobox-left uagb-infobox-stacked-tablet uagb-infobox-image-valign-middle uagb-infobox-enable-border-radius \"><div class=\"uagb-ifb-left-right-wrap\"><div class=\"uagb-ifb-image-icon-content uagb-ifb-imgicon-wrap\"><div class=\"uagb-ifb-image\"><div class=\"uagb-ifb-image-content\"><img decoding=\"async\" class=\"uagb-ifb-img-src\" src=\"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/wp-content\/uploads\/sites\/4\/2022\/05\/bandeira_mexico.jpg\" alt=\"\"\/><\/div><\/div><\/div><div class=\"uagb-ifb-content\"><div class=\"uagb-ifb-title-wrap\"><h3 class=\"uagb-ifb-title\">G\/TBT\/N\/MEX\/454\/Add. 2<br>Draft Mexican Official Standard PROY-NOM-241-SSA1-2018: Good manufacturing practices for medical devices<\/h3><\/div><div class=\"uagb-ifb-text-wrap\"><\/div><\/div><\/div><\/div><\/div>\n\n\n\n<p class=\"justified mb-3\">As part of our collaborative efforts to influence the development and improvement of technical regulations for medical devices, the Coalition prepared along with its members, the position paper regarding the new regulation on Good Manufacturing Practices of Medical Devices in Mexico, which will enter into force in June, 2023. The document can be <a href=\"\/regulatory-convergence\/wp-content\/uploads\/sites\/4\/2022\/06\/NOM241-20Dec21-IACRC-Position-04May22.pdf\" target=\"_blank\" rel=\"noreferrer noopener\">downloaded here<\/a>.<\/p>\n\n\n<a href=\"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/wp-content\/uploads\/sites\/4\/2022\/06\/NOM241-20Dec21-IACRC-Position-04May22.pdf\" class=\"pdfemb-viewer\" style=\"\" data-width=\"max\" data-height=\"max\" data-toolbar=\"both\" data-toolbar-fixed=\"off\">NOM241-20Dec21-IACRC-Position-04May22<\/a>\n<p class=\"wp-block-pdfemb-pdf-embedder-viewer\"><\/p>\n\n\n\n<section class=\"wp-block-uagb-section uagb-section__wrap uagb-section__background-undefined uagb-block-c660273d\"><div class=\"uagb-section__overlay\"><\/div><div class=\"uagb-section__inner-wrap\">\n<h3 class=\"wp-block-heading has-text-align-center mb-2 has-normal-font-size\" id=\"regulatory-coalition-principal-members\">REGULATORY COALITION PRINCIPAL MEMBERS<\/h3>\n\n\n<style 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width=\"240\" height=\"98\">\t<\/div>\n\t\t<\/div>\n<\/div>\n\t<div class=\"swiper-slide\">\n\t<div class=\"wpcp-single-item\">\n\t\t\t<div class=\"wpcp-slide-image\">\n\t\t<img loading=\"lazy\" decoding=\"async\" class=\"skip-lazy\" src=\"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/wp-content\/uploads\/sites\/4\/2021\/06\/member_advamed.jpg\" alt=\"member_advamed\" width=\"240\" height=\"65\">\t<\/div>\n\t\t<\/div>\n<\/div>\n\t\t\t<\/div>\n\t\t\t\t\t<div class=\"wpcp-swiper-dots swiper-pagination\"><\/div>\n\t\t\t\t<!-- If we need navigation buttons -->\n\t\t\t\t\t<div class=\"wpcp-prev-button swiper-button-prev\"><i class=\"fa fa-angle-left\"><\/i><\/div>\n\t\t\t<div class=\"wpcp-next-button swiper-button-next\"><i class=\"fa fa-angle-right\"><\/i><\/div>\n\t\t\t<\/div>\n\t<\/div>\n<\/div>\n\n<\/div><\/section>\n","protected":false},"excerpt":{"rendered":"<p>As part of our collaborative efforts to influence the development and improvement of technical regulations for medical devices, the Coalition prepared along with its members, the position paper regarding the new regulation on Good Manufacturing Practices of Medical Devices in Mexico, which will enter into force in June, 2023. The document can be downloaded here.<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":57,"menu_order":2,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"_uag_custom_page_level_css":"","footnotes":""},"class_list":["post-4145","page","type-page","status-publish","hentry","description-off"],"acf":[],"featured_image_src":null,"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.3 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Mexico - Regulatory Convergence<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/coalition-action\/positions\/mexico\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Mexico - Regulatory Convergence\" \/>\n<meta property=\"og:description\" content=\"As part of our collaborative efforts to influence the development and improvement of technical regulations for medical devices, the Coalition prepared along with its members, the position paper regarding the new regulation on Good Manufacturing Practices of Medical Devices in Mexico, which will enter into force in June, 2023. 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