{"id":2231,"date":"2021-07-06T13:17:13","date_gmt":"2021-07-06T13:17:13","guid":{"rendered":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/?page_id=2231"},"modified":"2021-07-29T13:00:08","modified_gmt":"2021-07-29T13:00:08","slug":"post-market-surveillance","status":"publish","type":"page","link":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/policy\/medical-device-sector-regulatory-convergence\/world-health-organization-documents\/post-market-surveillance\/","title":{"rendered":"Post Market Surveillance"},"content":{"rendered":"\n<figure class=\"wp-block-image size-large\"><img loading=\"lazy\" decoding=\"async\" width=\"187\" height=\"265\" src=\"http:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/wp-content\/uploads\/sites\/4\/2021\/07\/who_post_market_en.jpg\" alt=\"\" class=\"wp-image-2240\"\/><\/figure>\n\n\n\n<p class=\"mb-3\">In 2020 the World Health Organization launched the \u201cGuidance for post-market surveillance and market surveillance of medical devices, including in vitro diagnostics\u201d.<br>According to WHO, the document brings out a series of activities to be conducted by manufacturers \u201d to collect and evaluate experience gained from medical devices that have been placed on the market, and to identify the need to take any action.\u201d<\/p>\n\n\n\n<p>Read the document:<\/p>\n\n\n\n<div class=\"wp-block-buttons mb-3 is-layout-flex wp-block-buttons-is-layout-flex\">\n<div class=\"wp-block-button\"><a class=\"wp-block-button__link has-accent-background-color has-background\" href=\"\/regulatory-convergence\/wp-content\/uploads\/sites\/4\/2021\/07\/Post-market-surveillance-MDs-IVDs-eng.pdf\" target=\"_blank\" rel=\"noreferrer noopener\">English<\/a><\/div>\n\n\n\n<div class=\"wp-block-button\"><a class=\"wp-block-button__link has-accent-background-color has-background\" href=\"\/regulatory-convergence\/wp-content\/uploads\/sites\/4\/2021\/06\/Post-market-surveillance-MDs-IVDs-Espanol-Final-03May21.pdf\" target=\"_blank\" rel=\"noreferrer noopener\">Spanish<\/a><\/div>\n\n\n\n<div class=\"wp-block-button\"><a class=\"wp-block-button__link has-accent-background-color has-background\" href=\"\/regulatory-convergence\/wp-content\/uploads\/sites\/4\/2021\/07\/Post-market_surveillance_MDs_IVDs_Portuguese.pdf\" target=\"_blank\" rel=\"noreferrer noopener\">Portuguese<\/a><\/div>\n<\/div>\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 id=\"wp_carousel_dynamic_css118\">.sp-wp-carousel-free-id-118.wpcf-fancybox-wrapper .fancybox-bg{background: #0b0b0b;opacity: 0.8;}.sp-wp-carousel-free-id-118.wpcf-fancybox-wrapper .fancybox-navigation .fancybox-button .wpcp-fancybox-nav-arrow i {color: #ccc;}.sp-wp-carousel-free-id-118.wpcf-fancybox-wrapper .fancybox-navigation .fancybox-button .wpcp-fancybox-nav-arrow i:hover {color: #fff;}.sp-wp-carousel-free-id-118.wpcf-fancybox-wrapper .fancybox-navigation .fancybox-button {background: #1e1e1e;}.sp-wp-carousel-free-id-118.wpcf-fancybox-wrapper .fancybox-navigation .fancybox-button:hover {background: #1e1e1e;}#sp-wp-carousel-free-id-118 .wpcp-swiper-dots {margin: 40px 0px 0px 0px;}.wpcp-wrapper-118 .swiper-wrapper .swiper-slide-kenburn, .wpcp-wrapper-118 .swiper-wrapper, .wpcp-wrapper-118 .wpcpro-row{align-items: center;}#sp-wp-carousel-free-id-118 .wpcp-single-item {box-shadow: 0px 0px 0px 0px #dddddd;transition: all .3s;margin: 0px;}#sp-wp-carousel-free-id-118.swiper-flip .wpcp-single-item{margin: 0!important;}#sp-wp-carousel-free-id-118 .wpcp-single-item:hover {box-shadow: 0px 0px 0px 0px #dddddd;}#sp-wp-carousel-free-id-118.sp-wpcp-118 .wpcp-single-item {border: 0px solid transparent;}#sp-wp-carousel-free-id-118.sp-wpcp-118 .swiper-button-prev,#sp-wp-carousel-free-id-118.sp-wpcp-118 .swiper-button-next,#sp-wp-carousel-free-id-118.sp-wpcp-118 .swiper-button-prev:hover,#sp-wp-carousel-free-id-118.sp-wpcp-118 .swiper-button-next:hover {background: none;border: none;font-size: 30px;}#sp-wp-carousel-free-id-118.sp-wpcp-118 .swiper-button-prev i,#sp-wp-carousel-free-id-118.sp-wpcp-118 .swiper-button-next i {color: #aaa;}#sp-wp-carousel-free-id-118.sp-wpcp-118 .swiper-button-prev i:hover,#sp-wp-carousel-free-id-118.sp-wpcp-118 .swiper-button-next i:hover {color: #52b3d9;}#sp-wp-carousel-free-id-118.sp-wpcp-118 .wpcp-swiper-dots .swiper-pagination-bullet {background-color: #cccccc;}#sp-wp-carousel-free-id-118.sp-wpcp-118 .wpcp-swiper-dots .swiper-pagination-bullet.swiper-pagination-bullet-active {background-color: #52b3d9;} 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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>In 2020 the World Health Organization launched the \u201cGuidance for post-market surveillance and market surveillance of medical devices, including in vitro diagnostics\u201d.According to WHO, the document brings out a series of activities to be conducted by manufacturers \u201d to collect and evaluate experience gained from medical devices that have been placed on the market, and&hellip;<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":2221,"menu_order":3,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"_uag_custom_page_level_css":"","footnotes":""},"class_list":["post-2231","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>Post Market Surveillance - 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\/policy\/medical-device-sector-regulatory-convergence\/world-health-organization-documents\/post-market-surveillance\/\" 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