{"id":2272,"date":"2011-11-18T21:49:35","date_gmt":"2011-11-18T21:49:35","guid":{"rendered":"http:\/\/www.eisnersafety.com\/eisnersafetycom\/?p=2272"},"modified":"2011-11-18T21:49:35","modified_gmt":"2011-11-18T21:49:35","slug":"ghtf-to-morph-into-intl-medical-device-regulators-forum-imdrf","status":"publish","type":"post","link":"https:\/\/eisnersafety.com\/eisnersafetycom\/2011\/11\/18\/ghtf-to-morph-into-intl-medical-device-regulators-forum-imdrf\/","title":{"rendered":"GHTF to morph into Int&#8217;l Med Dvc Regulators&#8217; Forum (IMDRF)"},"content":{"rendered":"<p>The GHTF has been around for almost 20 years and is in the process of disbanding to become a more Regultor focused group called the International Medical Device Regulators&#8217; Forum (IMDRF).<\/p>\n<p>In the <a title=\"Eucomed 18 Nov 2011 Article on GHTF to become IMDRF\" href=\"http:\/\/www.eucomed.org\/newsletternews\/236\/124\/news\/2011\/11\/18\/GHTF-to-become-International-Medical-Device-Regulators-39-Forum-IMDRF\/\" target=\"_blank\" rel=\"noopener noreferrer\">Eucomed 18 Nov 2011 newsletter article<\/a> they say &#8220;In March 2011, the regulatory authorities of the &#8230; GHTF took the decision to disband the GHTF &#8230; to be replaced by a &#8216;regulator-led harmonisation and collaboration group.&#8217; &#8230; regulatory authorities felt that it was time to change the way the GHTF was operating so as to accelerate international medical device regulatory harmonisation.<\/p>\n<p>For more details see the <a title=\"Eucomed 18 Nov 2011 Article on GHTF to become IMDRF\" href=\"http:\/\/www.eucomed.org\/newsletternews\/236\/124\/news\/2011\/11\/18\/GHTF-to-become-International-Medical-Device-Regulators-39-Forum-IMDRF\/\" target=\"_blank\" rel=\"noopener noreferrer\">Eucomed newsletter article<\/a>.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>The GHTF has been around for almost 20 years and is in the process of disbanding to become a more Regultor focused group called the International Medical Device Regulators&#8217; Forum (IMDRF). In the Eucomed 18 Nov 2011 newsletter article they<\/p>\n","protected":false},"author":4,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_monsterinsights_skip_tracking":false,"_monsterinsights_sitenote_active":false,"_monsterinsights_sitenote_note":"","_monsterinsights_sitenote_category":0,"footnotes":""},"categories":[1],"tags":[246,247,471,472,330,174,312,372,149],"class_list":["post-2272","post","type-post","status-publish","format-standard","hentry","category-uncategorized","tag-ghtf","tag-global-harmonization-task-force","tag-imdrf","tag-international-medical-device-regulators-forum","tag-medical-device","tag-medical-device-industry","tag-medical-device-regulation","tag-medical-device-regulations","tag-medical-devices"],"_links":{"self":[{"href":"https:\/\/eisnersafety.com\/eisnersafetycom\/wp-json\/wp\/v2\/posts\/2272","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/eisnersafety.com\/eisnersafetycom\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/eisnersafety.com\/eisnersafetycom\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/eisnersafety.com\/eisnersafetycom\/wp-json\/wp\/v2\/users\/4"}],"replies":[{"embeddable":true,"href":"https:\/\/eisnersafety.com\/eisnersafetycom\/wp-json\/wp\/v2\/comments?post=2272"}],"version-history":[{"count":0,"href":"https:\/\/eisnersafety.com\/eisnersafetycom\/wp-json\/wp\/v2\/posts\/2272\/revisions"}],"wp:attachment":[{"href":"https:\/\/eisnersafety.com\/eisnersafetycom\/wp-json\/wp\/v2\/media?parent=2272"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/eisnersafety.com\/eisnersafetycom\/wp-json\/wp\/v2\/categories?post=2272"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/eisnersafety.com\/eisnersafetycom\/wp-json\/wp\/v2\/tags?post=2272"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}