{"id":9594,"date":"2025-10-28T10:11:59","date_gmt":"2025-10-28T10:11:59","guid":{"rendered":"https:\/\/zamra.co.zm\/vs\/new2025\/?page_id=9594"},"modified":"2026-06-25T12:56:17","modified_gmt":"2026-06-25T12:56:17","slug":"clinical-trials-regulation","status":"publish","type":"page","link":"https:\/\/zamra.co.zm\/vs\/new2025\/clinical-trials-regulation\/","title":{"rendered":"Clinical Trials &#8211; Regulation"},"content":{"rendered":"\t\t<div data-elementor-type=\"wp-page\" data-elementor-id=\"9594\" class=\"elementor elementor-9594\">\n\t\t\t\t<div class=\"elementor-element elementor-element-f5d91e9 e-flex e-con-boxed e-con e-parent\" data-id=\"f5d91e9\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t\t<div class=\"e-con-inner\">\n\t\t\t\t<div class=\"elementor-element elementor-element-72ce0c2 elementor-widget elementor-widget-heading\" data-id=\"72ce0c2\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\">Clinical Trials<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-ab4a806 elementor-widget elementor-widget-text-editor\" data-id=\"ab4a806\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<p class=\"PDq2pG_selectionAnchorContainer\" data-start=\"3424\" data-end=\"3728\">The Clinical Trials section is responsible for the review, authorization, and oversight of clinical research involving regulated products in Zambia. The Authority ensures that clinical trials are conducted ethically, scientifically, and in accordance with national and international regulatory standards.<\/p><p data-start=\"3730\" data-end=\"4056\">This section evaluates trial protocols, investigator qualifications, study documentation, and safety monitoring plans before authorizing the commencement of studies. Throughout the duration of approved trials, ZAMRA monitors compliance to ensure the rights, safety, dignity, and well-being of trial participants are protected.<\/p><p data-start=\"4058\" data-end=\"4254\">By facilitating responsible clinical research, the Authority supports scientific innovation and contributes to the development of safe and effective healthcare products for the Zambian population.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-f01299b elementor-icon-list--layout-traditional elementor-list-item-link-full_width elementor-widget elementor-widget-icon-list\" data-id=\"f01299b\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"icon-list.default\">\n\t\t\t\t\t\t\t<ul class=\"elementor-icon-list-items\">\n\t\t\t\t\t\t\t<li class=\"elementor-icon-list-item\">\n\t\t\t\t\t\t\t\t\t\t\t<a href=\"https:\/\/zamra.co.zm\/vs\/new2025\/wp-content\/uploads\/2026\/06\/Guidelines-on-Application-for-Clincal-Trial-Authorisation.pdf\" target=\"_blank\">\n\n\t\t\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-icon-list-icon\">\n\t\t\t\t\t\t\t<svg aria-hidden=\"true\" class=\"e-font-icon-svg e-far-file-pdf\" viewBox=\"0 0 384 512\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\"><path d=\"M369.9 97.9L286 14C277 5 264.8-.1 252.1-.1H48C21.5 0 0 21.5 0 48v416c0 26.5 21.5 48 48 48h288c26.5 0 48-21.5 48-48V131.9c0-12.7-5.1-25-14.1-34zM332.1 128H256V51.9l76.1 76.1zM48 464V48h160v104c0 13.3 10.7 24 24 24h104v288H48zm250.2-143.7c-12.2-12-47-8.7-64.4-6.5-17.2-10.5-28.7-25-36.8-46.3 3.9-16.1 10.1-40.6 5.4-56-4.2-26.2-37.8-23.6-42.6-5.9-4.4 16.1-.4 38.5 7 67.1-10 23.9-24.9 56-35.4 74.4-20 10.3-47 26.2-51 46.2-3.3 15.8 26 55.2 76.1-31.2 22.4-7.4 46.8-16.5 68.4-20.1 18.9 10.2 41 17 55.8 17 25.5 0 28-28.2 17.5-38.7zm-198.1 77.8c5.1-13.7 24.5-29.5 30.4-35-19 30.3-30.4 35.7-30.4 35zm81.6-190.6c7.4 0 6.7 32.1 1.8 40.8-4.4-13.9-4.3-40.8-1.8-40.8zm-24.4 136.6c9.7-16.9 18-37 24.7-54.7 8.3 15.1 18.9 27.2 30.1 35.5-20.8 4.3-38.9 13.1-54.8 19.2zm131.6-5s-5 6-37.3-7.8c35.1-2.6 40.9 5.4 37.3 7.8z\"><\/path><\/svg>\t\t\t\t\t\t<\/span>\n\t\t\t\t\t\t\t\t\t\t<span class=\"elementor-icon-list-text\">Guidelines-on-Application for Clinical Trial Authorisation<\/span>\n\t\t\t\t\t\t\t\t\t\t\t<\/a>\n\t\t\t\t\t\t\t\t\t<\/li>\n\t\t\t\t\t\t<\/ul>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t","protected":false},"excerpt":{"rendered":"<p>Clinical Trials The Clinical Trials section is responsible for the review, authorization, and oversight of clinical research involving regulated products in Zambia. The Authority ensures that clinical trials are conducted ethically, scientifically, and in accordance with national and international regulatory standards. This section evaluates trial protocols, investigator qualifications, study documentation, and safety monitoring plans before [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"om_disable_all_campaigns":false,"pagelayer_contact_templates":[],"_pagelayer_content":"","footnotes":""},"class_list":["post-9594","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/zamra.co.zm\/vs\/new2025\/wp-json\/wp\/v2\/pages\/9594","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/zamra.co.zm\/vs\/new2025\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/zamra.co.zm\/vs\/new2025\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/zamra.co.zm\/vs\/new2025\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/zamra.co.zm\/vs\/new2025\/wp-json\/wp\/v2\/comments?post=9594"}],"version-history":[{"count":5,"href":"https:\/\/zamra.co.zm\/vs\/new2025\/wp-json\/wp\/v2\/pages\/9594\/revisions"}],"predecessor-version":[{"id":9997,"href":"https:\/\/zamra.co.zm\/vs\/new2025\/wp-json\/wp\/v2\/pages\/9594\/revisions\/9997"}],"wp:attachment":[{"href":"https:\/\/zamra.co.zm\/vs\/new2025\/wp-json\/wp\/v2\/media?parent=9594"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}