{"id":2227,"date":"2021-07-06T13:16:40","date_gmt":"2021-07-06T13:16:40","guid":{"rendered":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/?page_id=2227"},"modified":"2021-07-29T12:47:08","modified_gmt":"2021-07-29T12:47:08","slug":"good-regulatory-practices","status":"publish","type":"page","link":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/policy\/medical-device-sector-regulatory-convergence\/world-health-organization-documents\/good-regulatory-practices\/","title":{"rendered":"Good Regulatory Practices"},"content":{"rendered":"\n<p class=\"mb-3\">The effective regulation of medical devices contributes to the strengthening of health systems. In order for a regulation to achieve its objectives, principles of good regulatory practices, whether legality, consistency, independence, impartiality, proportionality, flexibility, clarity, efficiency and transparency, must be observed in its development. The World Health Organization published the Good Regulatory Practices (GRP) document that \u201cprovides advice to establish and implement sound, affordable, efficient regulation of medical products as an important part of health system performance and sustainability.\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\/06\/GRP_WHO_TRS_1033-Annex-11.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\/GRP_WHO_TRS_1033-Annex-11_ESPANOL-Final-30Apr21.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\/06\/GRP_WHO_TRS_1033_Annex_11-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 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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>The effective regulation of medical devices contributes to the strengthening of health systems. In order for a regulation to achieve its objectives, principles of good regulatory practices, whether legality, consistency, independence, impartiality, proportionality, flexibility, clarity, efficiency and transparency, must be observed in its development. The World Health Organization published the Good Regulatory Practices (GRP) document&hellip;<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":2221,"menu_order":1,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"_uag_custom_page_level_css":"","footnotes":""},"class_list":["post-2227","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>Good Regulatory Practices - 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\/good-regulatory-practices\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Good Regulatory Practices - Regulatory Convergence\" \/>\n<meta property=\"og:description\" content=\"The effective regulation of medical devices contributes to the strengthening of health systems. 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