{"id":12718,"date":"2026-05-21T14:44:36","date_gmt":"2026-05-21T11:44:36","guid":{"rendered":"https:\/\/tlab.com.tr\/?page_id=12718"},"modified":"2026-05-21T16:13:07","modified_gmt":"2026-05-21T13:13:07","slug":"summary-of-safety-and-clinical-performance","status":"publish","type":"page","link":"https:\/\/tlab.com.tr\/en\/summary-of-safety-and-clinical-performance\/","title":{"rendered":"Summary of Safety and Clinical Performance"},"content":{"rendered":"<div data-elementor-type=\"wp-page\" data-elementor-id=\"12718\" class=\"elementor elementor-12718\">\n\t\t\t\t\t\t<section class=\"elementor-section elementor-top-section elementor-element elementor-element-0692815 elementor-section-boxed elementor-section-gap-beside-yes elementor-section-height-default elementor-section-height-default elementor-section-column-vertical-align-stretch\" data-id=\"0692815\" data-element_type=\"section\" data-e-type=\"section\">\n\t\t\t\t\t\t<div class=\"elementor-container elementor-column-gap-extended\">\n\t\t\t\t\t<div class=\"elementor-column elementor-col-100 elementor-top-column elementor-element elementor-element-4198a11\" data-id=\"4198a11\" data-element_type=\"column\" data-e-type=\"column\">\n\t\t\t<div class=\"elementor-widget-wrap elementor-element-populated\">\n\t\t\t\t\t\t<div class=\"elementor-element elementor-element-56214ca elementor-widget elementor-widget-text-editor\" data-id=\"56214ca\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t\t\t<h1 class=\"heading\">Summary of Safety and Clinical Performance<\/h1>\n<p><\/p>\n<table width=\"960\">\n<tbody>\n<tr>\n<td width=\"960\"><b>What is SSCP?<\/b><\/td>\n<\/tr>\n<tr>\n<td width=\"960\">The Summary of Safety and Clinical Performance (SSCP) is a requirement of the EU Medical Devices Regulation (EU MDR). SSCP provides a summary of the risks and benefits of certain devices and must be provided for all Class III and implantable devices (other than custom-made or investigational devices) and will be available in EUDAMED. The IFU shall contain all that is needed to directly find the SSCP in EUDAMED.<\/td>\n<\/tr>\n<tr>\n<td width=\"960\">&nbsp;<\/td>\n<\/tr>\n<tr>\n<td width=\"960\"><b>Purpose of SSCP<\/b><\/td>\n<\/tr>\n<tr>\n<td width=\"960\">The SSCP allows public access to an updated summary of clinical data and other information about the safety and clinical performance of the medical device. The SSCP will be an important source of information for intended users \u2013 both healthcare professionals\u2019 (HCPs) and, if relevant, for patients. It is one of several means intended to fulfill the objectives of EU MDR to ensure a robust, transparent, and sustainable regulatory framework and maintain a high level of safety.<\/td>\n<\/tr>\n<tr>\n<td width=\"960\">&nbsp;<\/td>\n<\/tr>\n<tr>\n<td width=\"960\"><b>SSCP Contents<\/b><\/td>\n<\/tr>\n<tr>\n<td width=\"960\">The SSCP contains easily understood and relevant information for HCPs and, when relevant, the public. This information is presented in separate sections and uses language and terms appropriate for the respective audience. Key information captured in the SSCP includes the description and intended use of the devices in scope, associated risks and warnings, an objective summary of existing and planned clinical data, and possible diagnostic or therapeutic alternatives. The SSCP is updated continuously through the products life cycle as new clinical data or other relevant information is available.<\/td>\n<\/tr>\n<tr>\n<td width=\"960\">&nbsp;<\/td>\n<\/tr>\n<tr>\n<td width=\"960\"><b>Accessing the SSCP<\/b><\/td>\n<\/tr>\n<tr>\n<td width=\"960\">After review and approval by a Notified Body, it is the Notified Body\u2019s responsibility to upload the SSCP into EUDAMED. At the latest when EUDAMED becomes mandatory the SSCP can be obtained from the Device section of EUDAMED on&nbsp;<a href=\"https:\/\/ec.europa.eu\/tools\/eudamed\" target=\"_blank\" rel=\"noopener\"><b>ec.europa.eu\/tools\/eudamed<\/b><\/a>. Prior to the EUDAMED mandatory usage date, the manufacturer makes the SSCP available upon request.<\/td>\n<\/tr>\n<tr>\n<td width=\"960\">Company Name: T-B\u0130YOTEKNOLOJ\u0130 LABORATUVAR ESTET\u0130K MED\u0130KAL KOZMET\u0130K SAN. T\u0130C. LTD. \u015eT\u0130.<\/td>\n<\/tr>\n<tr>\n<td width=\"960\">Actor ID\/SRN: TR-MF-000016403<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t<\/div>","protected":false},"excerpt":{"rendered":"<p>Summary of Safety and Clinical Performance What is SSCP? The Summary of Safety and Clinical Performance (SSCP) is a requirement of the EU Medical Devices Regulation (EU MDR). SSCP provides a summary of the risks and benefits of certain devices and must be provided for all Class III and implantable devices (other than custom-made or investigational devices) and will be available in EUDAMED. The IFU shall contain all that is needed to directly find the SSCP in EUDAMED. &nbsp; Purpose of SSCP The SSCP allows public access to an updated summary of clinical data and other information about the safety and clinical performance of the medical device. The SSCP will be an important source of information for intended users \u2013 both healthcare professionals\u2019 (HCPs) and, if relevant, for patients. It is one of several means intended to fulfill the objectives of EU MDR to ensure a robust, transparent, and sustainable regulatory framework and maintain a high level of safety. &nbsp; SSCP Contents The SSCP contains easily understood and relevant information for HCPs and, when relevant, the public. This information is presented in separate sections and uses language and terms appropriate for the respective audience. Key information captured in the SSCP includes the description and intended use of the devices in scope, associated risks and warnings, an objective summary of existing and planned clinical data, and possible diagnostic or therapeutic alternatives. The SSCP is updated continuously through the products life cycle as new clinical data or other relevant information is available. &nbsp; Accessing the SSCP After review and approval by a Notified Body, it is the Notified Body\u2019s responsibility to upload the SSCP into EUDAMED. At the latest when EUDAMED becomes mandatory the SSCP can be obtained from the Device section of EUDAMED on&nbsp;ec.europa.eu\/tools\/eudamed. Prior to the EUDAMED mandatory usage date, the manufacturer makes the SSCP available upon request. Company Name: T-B\u0130YOTEKNOLOJ\u0130 LABORATUVAR ESTET\u0130K MED\u0130KAL KOZMET\u0130K SAN. T\u0130C. LTD. \u015eT\u0130. Actor ID\/SRN: TR-MF-000016403<\/p>","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_monsterinsights_skip_tracking":false,"_monsterinsights_sitenote_active":false,"_monsterinsights_sitenote_note":"","_monsterinsights_sitenote_category":0,"_uf_show_specific_survey":0,"_uf_disable_surveys":false,"footnotes":""},"class_list":["post-12718","page","type-page","status-publish","hentry","post-no-thumbnail"],"_links":{"self":[{"href":"https:\/\/tlab.com.tr\/en\/wp-json\/wp\/v2\/pages\/12718","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/tlab.com.tr\/en\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/tlab.com.tr\/en\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/tlab.com.tr\/en\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/tlab.com.tr\/en\/wp-json\/wp\/v2\/comments?post=12718"}],"version-history":[{"count":27,"href":"https:\/\/tlab.com.tr\/en\/wp-json\/wp\/v2\/pages\/12718\/revisions"}],"predecessor-version":[{"id":12748,"href":"https:\/\/tlab.com.tr\/en\/wp-json\/wp\/v2\/pages\/12718\/revisions\/12748"}],"wp:attachment":[{"href":"https:\/\/tlab.com.tr\/en\/wp-json\/wp\/v2\/media?parent=12718"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}