{"id":15377,"date":"2026-06-17T15:41:14","date_gmt":"2026-06-17T10:11:14","guid":{"rendered":"https:\/\/operonstrategist.com\/?p=15377"},"modified":"2026-06-17T15:41:14","modified_gmt":"2026-06-17T10:11:14","slug":"understanding-the-prrc-under-eu-mdr-and-ivdr","status":"publish","type":"post","link":"https:\/\/operonstrategist.com\/za-en\/understanding-the-prrc-under-eu-mdr-and-ivdr\/","title":{"rendered":"Understanding The PRRC Under EU MDR and IVDR"},"content":{"rendered":"\t\t<div data-elementor-type=\"wp-post\" data-elementor-id=\"15377\" class=\"elementor elementor-15377\" data-elementor-post-type=\"post\">\n\t\t\t\t<div class=\"elementor-element elementor-element-6888d4cc e-flex e-con-boxed e-con e-parent\" data-id=\"6888d4cc\" 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-5febfb30 elementor-widget elementor-widget-heading\" data-id=\"5febfb30\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t\t<h1 class=\"elementor-heading-title elementor-size-default\">Understanding The PRRC Under EU MDR and IVDR<\/h1>\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t<div class=\"elementor-element elementor-element-549198d e-flex e-con-boxed e-con e-parent\" data-id=\"549198d\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t\t<div class=\"e-con-inner\">\n\t\t<div class=\"elementor-element elementor-element-7f60cd1 e-con-full e-flex e-con e-child\" data-id=\"7f60cd1\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t<div class=\"elementor-element elementor-element-1759255b elementor-widget elementor-widget-heading\" data-id=\"1759255b\" 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\">Introduction to PRRC under EU MDR\n<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-7fdb9aef elementor-widget elementor-widget-text-editor\" data-id=\"7fdb9aef\" 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><span style=\"font-weight: 400;\">The EU Medical Device Regulation (MDR 2017\/745) and In Vitro Diagnostic Regulation (IVDR 2017\/746) have dramatically transformed the regulatory framework for medical devices and IVDs in Europe. Among the major changes is the introduction of a crucial new role the Person Responsible for Regulatory Compliance (PRRC).<\/span><span style=\"font-weight: 400;\"><br \/><\/span><span style=\"font-weight: 400;\">In this blog, we delve into the importance of the PRRC, their key responsibilities, and why this role is essential for ensuring regulatory compliance under EU MDR and IVDR.<\/span><\/p><p><span style=\"font-weight: 400;\">Read more about <\/span><a href=\"https:\/\/operonstrategist.com\/understanding-the-responsibilities-of-economic-operators-under-the-eu-mdr-2017-745\/\"><span style=\"font-weight: 400;\">Understanding the Responsibilities of Economic Operators Under the EU MDR 2017\/745<\/span><\/a><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t<div class=\"elementor-element elementor-element-4d4fdbfb e-con-full e-flex e-con e-child\" data-id=\"4d4fdbfb\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t<div class=\"elementor-element elementor-element-75572d4b e-con-full e-flex e-con e-child\" data-id=\"75572d4b\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t<div class=\"elementor-element elementor-element-45cd21ff elementor-widget elementor-widget-heading\" data-id=\"45cd21ff\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t\t<h4 class=\"elementor-heading-title elementor-size-default\">Regulatory Excellence for Global Medical Device Markets\n<\/h4>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-2825c191 elementor-widget elementor-widget-wpforms\" data-id=\"2825c191\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"wpforms.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t<div class=\"wpforms-container wpforms-container-full wpforms-render-modern\" id=\"wpforms-6203\"><form id=\"wpforms-form-6203\" class=\"wpforms-validate wpforms-form wpforms-ajax-form\" 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required><\/div>\t\t<div id=\"wpforms-6203-field_5-container\"\n\t\t\tclass=\"wpforms-field wpforms-field-text\"\n\t\t\tdata-field-type=\"text\"\n\t\t\tdata-field-id=\"5\"\n\t\t\t>\n\t\t\t<label class=\"wpforms-field-label\" for=\"wpforms-6203-field_5\" >Name Text Email<\/label>\n\t\t\t<input type=\"text\" id=\"wpforms-6203-field_5\" class=\"wpforms-field-medium\" name=\"wpforms[fields][5]\" >\n\t\t<\/div>\n\t\t<div id=\"wpforms-6203-field_2-container\" class=\"wpforms-field wpforms-field-email\" data-field-id=\"2\"><label class=\"wpforms-field-label wpforms-label-hide\" for=\"wpforms-6203-field_2\" aria-hidden=\"false\">Email <span class=\"wpforms-required-label\" aria-hidden=\"true\">*<\/span><\/label><input type=\"email\" id=\"wpforms-6203-field_2\" class=\"wpforms-field-large wpforms-field-required\" name=\"wpforms[fields][2]\" placeholder=\"Email*\" spellcheck=\"false\" aria-errormessage=\"wpforms-6203-field_2-error\" required><\/div><div id=\"wpforms-6203-field_3-container\" 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placeholder=\"Message\" aria-errormessage=\"wpforms-6203-field_4-error\" required><\/textarea><\/div><script>\n\t\t\t\t( function() {\n\t\t\t\t\tconst style = document.createElement( 'style' );\n\t\t\t\t\tstyle.appendChild( document.createTextNode( '#wpforms-6203-field_5-container { position: absolute !important; overflow: hidden !important; display: inline !important; height: 1px !important; width: 1px !important; z-index: -1000 !important; padding: 0 !important; } #wpforms-6203-field_5-container input { visibility: hidden; } #wpforms-conversational-form-page #wpforms-6203-field_5-container label { counter-increment: none; }' ) );\n\t\t\t\t\tdocument.head.appendChild( style );\n\t\t\t\t\tdocument.currentScript?.remove();\n\t\t\t\t} )();\n\t\t\t<\/script><\/div><!-- .wpforms-field-container --><div class=\"wpforms-recaptcha-container wpforms-is-recaptcha wpforms-is-recaptcha-type-v3\" ><input type=\"hidden\" name=\"wpforms[recaptcha]\" value=\"\"><\/div><div class=\"wpforms-submit-container\" ><input type=\"hidden\" name=\"wpforms[id]\" value=\"6203\"><input type=\"hidden\" name=\"page_title\" value=\"\"><input type=\"hidden\" name=\"page_url\" value=\"https:\/\/operonstrategist.com\/za-en\/wp-json\/wp\/v2\/posts\/15377\"><input type=\"hidden\" name=\"url_referer\" value=\"\"><button type=\"submit\" name=\"wpforms[submit]\" id=\"wpforms-submit-6203\" class=\"wpforms-submit\" data-alt-text=\"Sending...\" data-submit-text=\"Submit\" aria-live=\"assertive\" value=\"wpforms-submit\">Submit<\/button><img decoding=\"async\" src=\"https:\/\/operonstrategist.com\/wp-content\/plugins\/wpforms\/assets\/images\/submit-spin.svg\" class=\"wpforms-submit-spinner\" style=\"display: none;\" width=\"26\" height=\"26\" alt=\"Loading\"><\/div><\/form><\/div>  <!-- .wpforms-container -->\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t<div class=\"elementor-element elementor-element-cbf0ae6 e-flex e-con-boxed e-con e-parent\" data-id=\"cbf0ae6\" 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-76429123 elementor-widget elementor-widget-heading\" data-id=\"76429123\" 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\">Who Needs a PRRC?\n<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-589f67a3 elementor-widget elementor-widget-text-editor\" data-id=\"589f67a3\" 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><span style=\"font-weight: 400;\">Article 15 of the EU MDR and IVDR mandates that manufacturers and non-EEA manufacturers\u2019 EU-authorized representatives appoint a Person Responsible for Regulatory Compliance (PRRC). While legacy devices are exempt from this requirement, many manufacturers include them under PRRC oversight for simplicity.\u00a0\u00a0<\/span><\/p><p><span style=\"font-weight: 400;\">Non-EEA manufacturers must confirm their EU authorized representative appoints a qualified PRRC, but the same individual cannot serve as PRRC for both parties. Companies with multiple legal manufacturers must assign a PRRC for each entity. <\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-cb49d1a elementor-widget elementor-widget-heading\" data-id=\"cb49d1a\" 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\">12 Things You Need to Know About the PRRC under EU MDR and IVDR\n<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-725bfed elementor-widget elementor-widget-text-editor\" data-id=\"725bfed\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<ol><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\"><strong>Legal Mandate<\/strong>: The PRRC role is mandated under EU MDR (EU 2017\/745) and IVDR (EU 2017\/746) as per Article 15.\u00a0<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\"><strong>Qualifications<\/strong>: A PRRC must possess a relevant university degree or equivalent certification or have at least four years of professional experience in regulatory affairs or <\/span><span style=\"font-weight: 400;\">quality management.<\/span><span style=\"font-weight: 400;\">\u00a0<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\"><strong>Availability<\/strong>: The PRRC must be permanently and continuously available to manufacturers and authorized representatives, ensuring access to all relevant documents and records necessary for fulfilling their duties.\u00a0<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\"><strong>Responsibilities<\/strong>: The PRRC verifies that technical documentation and EU declarations of conformity are up to date. They also oversee compliance with Post-Market Surveillance (PMS) systems, reporting obligations (Articles 87\u201391 for MDR, 82\u201386 for IVDR), and investigational device conformity statements (Annex XV).\u00a0<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\"><strong>Micro and Small Manufacturers<\/strong>: Micro and small manufacturers may subcontract the PRRC role if the designated individual meets the necessary qualifications and is permanently available, as outlined in MDCG 2019-7.\u00a0<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\"><strong>Authorized Representatives<\/strong>: For authorized representatives, the PRRC ensures manufacturer compliance, verifies the completeness of technical documentation, and registers required information in EUDAMED as per Article 11(3).\u00a0<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\"><strong>Documentation<\/strong>: PRRC responsibilities and tasks must be clearly documented and accepted by the individual. Senior management must support the PRRC with the necessary authority and resources.\u00a0<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\"><strong>Independence<\/strong>: The PRRC must maintain independence to ensure impartial oversight. A single PRRC cannot serve as both the manufacturer\u2019s and the authorized representative\u2019s PRRC simultaneously.\u00a0<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\"><strong>Parent Companies and Virtual Manufacturers<\/strong>: Each legal manufacturer under a parent company must have its own PRRC. For virtual manufacturers, the PRRC must ensure that the OEM complies with MDR\/IVDR requirements.\u00a0<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\"><strong>Risk-Based Approach<\/strong>: The PRRC\u2019s duties should align with the risk class of the devices, ensuring a proportional and risk-based oversight.\u00a0<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\"><strong>Liability<\/strong>: The PRRC is not personally liable for compliance failures; their role is to ensure that regulatory activities are performed in accordance with requirements.\u00a0<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\"><strong>Registration<\/strong>: PRRC details, including name and contact information, must be registered in EUDA-MED to ensure traceability and accountability. <\/span><\/li><\/ol>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-f88575c elementor-widget elementor-widget-heading\" data-id=\"f88575c\" 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\">Key Responsibilities of the PRRC<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-f178cf2 elementor-widget elementor-widget-text-editor\" data-id=\"f178cf2\" 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><span style=\"font-weight: 400;\">The PRRC is entrusted with several critical responsibilities, ensuring the compliance and safety of medical devices and in vitro diagnostics. These include:\u00a0<\/span><\/p><ol><li style=\"list-style-type: none;\"><ol><li style=\"font-weight: 400;\" aria-level=\"1\"><strong>Device Conformity<br \/><span style=\"font-weight: 400;\">Ensuring that the conformity of devices is checked appropriately in accordance with the quality management system before the devices are released. <\/span><i><span style=\"font-weight: 400;\">(Art. 10(9))<br \/><\/span><\/i> <br \/><\/strong><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><strong><strong>Technical Documentation and Declaration of Conformity<br \/><\/strong><\/strong><p><span style=\"font-weight: 400;\">Ensuring the preparation and maintenance of the Technical Documentation and the EU Declaration of Conformity. <\/span><i><span style=\"font-weight: 400;\">(Art. 10(6))<\/span><\/i><span style=\"font-weight: 400;\">\u00a0<\/span><\/p><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><strong><strong><a href=\"https:\/\/operonstrategist.com\/services\/post-market-surveillance\/\">Post-Market Surveillance (PMS)<\/a><br \/><\/strong><\/strong><p><span style=\"font-weight: 400;\">Ensuring compliance with PMS obligations in accordance with Article 10(10). This includes the implementation and continuous updating of the PMS system as outlined in Article 83 and Annex III.\u00a0<\/span><\/p><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><strong><strong>Reporting Obligations<br \/><\/strong><\/strong><p><span style=\"font-weight: 400;\">Ensuring the proper functioning of systems for recording and reporting incidents and field safety corrective actions, as required by Articles 87 to 91.\u00a0<\/span><\/p><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><strong><strong>Investigational Devices<br \/><\/strong><\/strong><p><span style=\"font-weight: 400;\">In the case of investigational devices, the PRRC must confirm compliance with General Safety and Performance Requirements (GSPR) and ensure that all health and safety precautions for subjects are in place. <\/span><i><span style=\"font-weight: 400;\">(Section 4.1 of Chapter II of Annex XV).<\/span><\/i><span style=\"font-weight: 400;\">\u00a0<\/span><\/p><\/li><\/ol><\/li><\/ol>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-77ddcb7 elementor-widget elementor-widget-heading\" data-id=\"77ddcb7\" 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\">Role of Operon Strategist\n<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-e40d320 elementor-widget elementor-widget-text-editor\" data-id=\"e40d320\" 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><span style=\"font-weight: 400;\">Operon Strategist helps manufacturers and stakeholders navigate EU MDR and IVDR requirements, including PRRC responsibilities, ensuring smooth compliance. With deep regulatory expertise and a commitment to excellence, they enable clients to confidently manage global medical device regulations.\u00a0<\/span><\/p><p><span style=\"font-weight: 400;\">Operon Strategist provides end-to-end support for <\/span><a href=\"https:\/\/operonstrategist.com\/services\/\"><span style=\"font-weight: 400;\">regulatory approvals<\/span><\/a><span style=\"font-weight: 400;\"> like <\/span><a href=\"https:\/\/operonstrategist.com\/services\/regulatory-approvals\/ce-marking\/\"><span style=\"font-weight: 400;\">European CE marking<\/span><\/a><span style=\"font-weight: 400;\">, <\/span><a href=\"https:\/\/operonstrategist.com\/services\/regulatory-approvals\/fda-510k\/\"><span style=\"font-weight: 400;\">FDA 510(k)<\/span><\/a><span style=\"font-weight: 400;\">, <\/span><a href=\"https:\/\/operonstrategist.com\/services\/regulatory-approvals\/cdsco-registration\/cdsco-import-license\/\"><span style=\"font-weight: 400;\">Indian CDSCO import registration<\/span><\/a><span style=\"font-weight: 400;\">, <\/span><a href=\"https:\/\/operonstrategist.com\/services\/regulatory-approvals\/medical-device-registration-in-saudi-arabia\/\"><span style=\"font-weight: 400;\">SFDA<\/span><\/a><span style=\"font-weight: 400;\"> and <\/span><a href=\"https:\/\/operonstrategist.com\/elevateplus\/ukca-marking\/\"><span style=\"font-weight: 400;\">UKCA<\/span><\/a><span style=\"font-weight: 400;\"> compliance. They assist in setting up manufacturing units with <\/span><a href=\"https:\/\/operonstrategist.com\/services\/turnkey-project\/manufacturing-facility\/\"><span style=\"font-weight: 400;\">Facility layout designing<\/span><\/a><span style=\"font-weight: 400;\">, cleanroom design, machine validation and facility compliance as per all regulatory norms, ensuring quality through <\/span><a href=\"https:\/\/operonstrategist.com\/elevateplus\/quality-management-system-qms\/\"><span style=\"font-weight: 400;\">ISO 13485<\/span><\/a><span style=\"font-weight: 400;\">, <\/span><a href=\"https:\/\/operonstrategist.com\/elevateplus\/us-fda-510k-qmsr-registration\/\"><span style=\"font-weight: 400;\">FDA QSR<\/span><\/a><span style=\"font-weight: 400;\">, and <\/span><span style=\"font-weight: 400;\">MDSAP<\/span><span style=\"font-weight: 400;\"> compliance and all regulatory approvals.\u00a0\u00a0<\/span><\/p><p><span style=\"font-weight: 400;\">Our expertise extends to design and development, including technical documentation and risk management, while also offering tailored training and consultation for regulatory and licensing needs.\u00a0<\/span><\/p>\t\t\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>Introduction to PRRC under EU MDR The EU Medical Device Regulation (MDR 2017\/745) and In Vitro Diagnostic Regulation (IVDR 2017\/746) have dramatically transformed the regulatory framework for medical devices and IVDs in Europe. Among the major changes is the introduction of a crucial new role the Person Responsible for Regulatory Compliance (PRRC). In this blog, [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":15545,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[55],"tags":[],"class_list":["post-15377","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-regulatory"],"_links":{"self":[{"href":"https:\/\/operonstrategist.com\/za-en\/wp-json\/wp\/v2\/posts\/15377","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/operonstrategist.com\/za-en\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/operonstrategist.com\/za-en\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/operonstrategist.com\/za-en\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/operonstrategist.com\/za-en\/wp-json\/wp\/v2\/comments?post=15377"}],"version-history":[{"count":1,"href":"https:\/\/operonstrategist.com\/za-en\/wp-json\/wp\/v2\/posts\/15377\/revisions"}],"predecessor-version":[{"id":15546,"href":"https:\/\/operonstrategist.com\/za-en\/wp-json\/wp\/v2\/posts\/15377\/revisions\/15546"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/operonstrategist.com\/za-en\/wp-json\/wp\/v2\/media\/15545"}],"wp:attachment":[{"href":"https:\/\/operonstrategist.com\/za-en\/wp-json\/wp\/v2\/media?parent=15377"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/operonstrategist.com\/za-en\/wp-json\/wp\/v2\/categories?post=15377"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/operonstrategist.com\/za-en\/wp-json\/wp\/v2\/tags?post=15377"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}