{"id":65999,"date":"2026-02-23T23:23:44","date_gmt":"2026-02-23T23:23:44","guid":{"rendered":"https:\/\/www.veeva.com\/medtech\/?page_id=65999"},"modified":"2026-08-06T14:43:39","modified_gmt":"2026-08-06T14:43:39","slug":"speakers","status":"publish","type":"page","link":"https:\/\/www.veeva.com\/medtech\/eu-summit-2026\/speakers\/","title":{"rendered":"EU Summit 2026 &#8211; Speakers"},"content":{"rendered":"<!-- page_id: 65999 -->\n\n<link rel='stylesheet' id='veeva-2024-bundle-css' href='https:\/\/www.veeva.com\/wp-content\/themes\/veeva2015\/assets\/css\/bundle.min.css?ver=1755188017' media='all' \/>\n\n<div class=\"veeva-2024\">\n\n<!-- Speakers Start -->\n<section class=\"people-events people-events--light\">\n\t<div class=\"copy-container container copy-container--center copy-container--eyebrow-gradient\">\n\t\t<h6><span class=\"icon ready\" data-icon=\"annoncement-megaphone\" style=\"--icon: url('/medtech/wp-json/wp/v2/pages/65999/wp-content/themes/medtech2021/assets/svg/icons/annoncement-megaphone.svg');\"><\/span>2026 Speakers<\/h6>\n\t<\/div>\n\t<div class=\"people-events__cards container\">\n\n\t\t<div class=\"person-card-events person-card-events--light\" data-bs-toggle=\"modal\" data-bs-target=\"#abhi-lee-steve\">\n    <img decoding=\"async\" class=\"person-card-events__thumbnail\" src=\"https:\/\/www.veeva.com\/medtech\/wp-content\/uploads\/2026\/08\/Steve-Lee-1.png\" alt=\"\" \/><\/p>\n<h6>Steve Lee<\/h6>\n<p class=\"person-card-events__company\">ABHI<\/p>\n<p>Head of Regulatory<\/p>\n<\/div>\n<div id=\"abhi-lee-steve\" class=\"modal fade speaker-modal speaker-modal--light\" tabindex=\"-1\">\n<div class=\"modal-dialog modal-lg modal-dialog-scrollable\">\n<div class=\"modal-content\">\n<div class=\"modal-body\">\n                <button type=\"button\" class=\"modal-btn-close\" data-bs-dismiss=\"modal\" aria-label=\"Close\"><br \/>\n                    <span class=\"icon ready\" data-icon=\"close\" style=\"--icon: url('/medtech/wp-json/wp/v2/pages/65999/wp-content/themes/veeva2015/assets/svg/icons/close.svg');\"><\/span><br \/>\n                <\/button><\/p>\n<div class=\"modal-speaker-info\">\n<div class=\"avatar-thumbnail\">\n                        <img decoding=\"async\" src=\"https:\/\/www.veeva.com\/medtech\/wp-content\/uploads\/2026\/08\/Steve-Lee-1.png\" alt=\"\" \/>\n                    <\/div>\n<div class=\"modal-speaker-info__text\">\n<h5 class=\"speaker-name\">Steve Lee<\/h5>\n<p>\n                            <span class=\"speaker-company\">ABHI<\/span><br \/>\n                            <span class=\"speaker-position\"> Head of Regulatory <\/span>\n                        <\/p>\n<\/p><\/div>\n<\/p><\/div>\n<hr class=\"modal-inner-separator\" \/>\n<div class=\"modal-speaker-bio\">\n<p>\n                        Steve leads ABHI&#8217;s regulatory policy for IVDs and digital health, representing members with the MHRA and IMDRF to drive global regulatory convergence. He brings over two decades of experience from the MHRA, where he also chaired the European Commission\u2019s IVD working group during the development of the IVDR.\n                    <\/p>\n<\/p><\/div>\n<div class=\"modal-speaker-session\">\n<h5>Sessions<\/h5>\n<hr \/>\n<p>                    <a class=\"modal-speaker-session__item\" href=\"https:\/\/www.veeva.com\/medtech\/eu-summit-2026\/agenda\/#j-31\"><\/p>\n<h6>ABHI and GMED: 10 Essentials for a Simplified Digital Regulatory Future<\/h6>\n<p>11\/4\/2026 9:00 a.m.<\/p>\n<p>    <span class=\"forward-arrow\"><\/span><br \/>\n<\/a><\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/div>\n<div class=\"person-card-events person-card-events--light\" data-bs-toggle=\"modal\" data-bs-target=\"#becton-dickinson-and-company-zeigler-christy\">\n    <img decoding=\"async\" class=\"person-card-events__thumbnail\" src=\"https:\/\/www.veeva.com\/medtech\/wp-content\/uploads\/2026\/03\/Zeigler_Christy-2.png\" alt=\"\" \/><\/p>\n<h6>Christy Zeigler<\/h6>\n<p class=\"person-card-events__company\">Becton Dickinson and Company<\/p>\n<p>Director, Clinical Data Management<\/p>\n<\/div>\n<div id=\"becton-dickinson-and-company-zeigler-christy\" class=\"modal fade speaker-modal speaker-modal--light\" tabindex=\"-1\">\n<div class=\"modal-dialog modal-lg modal-dialog-scrollable\">\n<div class=\"modal-content\">\n<div class=\"modal-body\">\n                <button type=\"button\" class=\"modal-btn-close\" data-bs-dismiss=\"modal\" aria-label=\"Close\"><br \/>\n                    <span class=\"icon ready\" data-icon=\"close\" style=\"--icon: url('/medtech/wp-json/wp/v2/pages/65999/wp-content/themes/veeva2015/assets/svg/icons/close.svg');\"><\/span><br \/>\n                <\/button><\/p>\n<div class=\"modal-speaker-info\">\n<div class=\"avatar-thumbnail\">\n                        <img decoding=\"async\" src=\"https:\/\/www.veeva.com\/medtech\/wp-content\/uploads\/2026\/03\/Zeigler_Christy-2.png\" alt=\"\" \/>\n                    <\/div>\n<div class=\"modal-speaker-info__text\">\n<h5 class=\"speaker-name\">Christy Zeigler<\/h5>\n<p>\n                            <span class=\"speaker-company\">Becton Dickinson and Company<\/span><br \/>\n                            <span class=\"speaker-position\"> Director, Clinical Data Management <\/span>\n                        <\/p>\n<\/p><\/div>\n<\/p><\/div>\n<hr class=\"modal-inner-separator\" \/>\n<div class=\"modal-speaker-bio\">\n<p>\n                        Christy has 25+ years of experience across the pharmaceutical and medical device industries in sponsor and CRO settings. For nearly five years, she has partnered with ³Ô¹Ï±¬ÁÏ and leads a team of clinical data managers and database programmers supporting multiple BD business units. Christy delivers end-to-end data management\u2014from study start-up through database lock\u2014by championing interoperable workflows (EDC, eCOA, CDB) that reduce burden, accelerate insights, and strengthen compliance.<\/p>\n<\/p><\/div>\n<div class=\"modal-speaker-session\">\n<h5>Sessions<\/h5>\n<hr \/>\n<p>                    <a class=\"modal-speaker-session__item\" href=\"https:\/\/www.veeva.com\/medtech\/eu-summit-2026\/agenda\/#j-18\"><\/p>\n<h6>BD: Enhancing Patient Engagement and Data Quality<br \/>\n<\/h6>\n<p>11\/3\/2026 2:45 p.m.<\/p>\n<p>    <span class=\"forward-arrow\"><\/span><br \/>\n<\/a><\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/div>\n<div class=\"person-card-events person-card-events--light\" data-bs-toggle=\"modal\" data-bs-target=\"#bsi-holborow-richard\">\n    <img decoding=\"async\" class=\"person-card-events__thumbnail\" src=\"https:\/\/www.veeva.com\/medtech\/wp-content\/uploads\/2026\/08\/Image-8.png\" alt=\"\" \/><\/p>\n<h6>Richard Holborow<\/h6>\n<p class=\"person-card-events__company\">BSI<\/p>\n<p>Head of Clinical Compliance<\/p>\n<\/div>\n<div id=\"bsi-holborow-richard\" class=\"modal fade speaker-modal speaker-modal--light\" tabindex=\"-1\">\n<div class=\"modal-dialog modal-lg modal-dialog-scrollable\">\n<div class=\"modal-content\">\n<div class=\"modal-body\">\n                <button type=\"button\" class=\"modal-btn-close\" data-bs-dismiss=\"modal\" aria-label=\"Close\"><br \/>\n                    <span class=\"icon ready\" data-icon=\"close\" style=\"--icon: url('/medtech/wp-json/wp/v2/pages/65999/wp-content/themes/veeva2015/assets/svg/icons/close.svg');\"><\/span><br \/>\n                <\/button><\/p>\n<div class=\"modal-speaker-info\">\n<div class=\"avatar-thumbnail\">\n                        <img decoding=\"async\" src=\"https:\/\/www.veeva.com\/medtech\/wp-content\/uploads\/2026\/08\/Image-8.png\" alt=\"\" \/>\n                    <\/div>\n<div class=\"modal-speaker-info__text\">\n<h5 class=\"speaker-name\">Richard Holborow<\/h5>\n<p>\n                            <span class=\"speaker-company\">BSI<\/span><br \/>\n                            <span class=\"speaker-position\"> Head of Clinical Compliance <\/span>\n                        <\/p>\n<\/p><\/div>\n<\/p><\/div>\n<hr class=\"modal-inner-separator\" \/>\n<div class=\"modal-speaker-bio\">\n<p>\n                        With 16 years of NHS experience as a cardiac clinical physiologist, Richard joined BSI in 2018, where he is now head of clinical compliance. He is also involved in EU Medical Device Coordination Group (MDCG) working groups.\n                    <\/p>\n<\/p><\/div>\n<div class=\"modal-speaker-session\">\n<h5>Sessions<\/h5>\n<hr \/>\n<p>                    <a class=\"modal-speaker-session__item\" href=\"https:\/\/www.veeva.com\/medtech\/eu-summit-2026\/agenda\/#j-2\"><\/p>\n<h6>BSI and Teleflex: Leveraging Clinical Evidence and RWD to Accelerate Market Access<\/h6>\n<p>11\/3\/2026 9:45 a.m.<\/p>\n<p>    <span class=\"forward-arrow\"><\/span><br \/>\n<\/a><\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/div>\n<div class=\"person-card-events person-card-events--light\" data-bs-toggle=\"modal\" data-bs-target=\"#bsi-laan-alex\">\n    <img decoding=\"async\" class=\"person-card-events__thumbnail\" src=\"https:\/\/www.veeva.com\/medtech\/wp-content\/uploads\/2026\/08\/Image-12.png\" alt=\"\" \/><\/p>\n<h6>Alex Laan<\/h6>\n<p class=\"person-card-events__company\">BSI<\/p>\n<p>Head of IVD Notified Body<\/p>\n<\/div>\n<div id=\"bsi-laan-alex\" class=\"modal fade speaker-modal speaker-modal--light\" tabindex=\"-1\">\n<div class=\"modal-dialog modal-lg modal-dialog-scrollable\">\n<div class=\"modal-content\">\n<div class=\"modal-body\">\n                <button type=\"button\" class=\"modal-btn-close\" data-bs-dismiss=\"modal\" aria-label=\"Close\"><br \/>\n                    <span class=\"icon ready\" data-icon=\"close\" style=\"--icon: url('/medtech/wp-json/wp/v2/pages/65999/wp-content/themes/veeva2015/assets/svg/icons/close.svg');\"><\/span><br \/>\n                <\/button><\/p>\n<div class=\"modal-speaker-info\">\n<div class=\"avatar-thumbnail\">\n                        <img decoding=\"async\" src=\"https:\/\/www.veeva.com\/medtech\/wp-content\/uploads\/2026\/08\/Image-12.png\" alt=\"\" \/>\n                    <\/div>\n<div class=\"modal-speaker-info__text\">\n<h5 class=\"speaker-name\">Alex Laan<\/h5>\n<p>\n                            <span class=\"speaker-company\">BSI<\/span><br \/>\n                            <span class=\"speaker-position\"> Head of IVD Notified Body <\/span>\n                        <\/p>\n<\/p><\/div>\n<\/p><\/div>\n<hr class=\"modal-inner-separator\" \/>\n<div class=\"modal-speaker-bio\">\n<p>\n                        Alex is head of notified body IVD at BSI.  As a bioprocess engineer, he brings over 12 years of notified body leadership from DEKRA and KEMA, complemented by extensive QA\/RA industry experience and four years as a regulatory consultant.\n                    <\/p>\n<\/p><\/div>\n<div class=\"modal-speaker-session\">\n<h5>Sessions<\/h5>\n<hr \/>\n<p>                    <a class=\"modal-speaker-session__item\" href=\"https:\/\/www.veeva.com\/medtech\/eu-summit-2026\/agenda\/#j-3\"><\/p>\n<h6>BSI, DNV Product Assurance, and MHRA: Continuous Compliance in a Rapidly Changing Regulatory Landscape<\/h6>\n<p>11\/3\/2026 9:45 a.m.<\/p>\n<p>    <span class=\"forward-arrow\"><\/span><br \/>\n<\/a><\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/div>\n<div class=\"person-card-events person-card-events--light\" data-bs-toggle=\"modal\" data-bs-target=\"#coloplast-yildiran-handan\">\n    <img decoding=\"async\" class=\"person-card-events__thumbnail\" src=\"https:\/\/www.veeva.com\/medtech\/wp-content\/uploads\/2026\/08\/Handan-Yildiran-600x390-1.png\" alt=\"\" \/><\/p>\n<h6>Handan Yildiran<\/h6>\n<p class=\"person-card-events__company\">Coloplast<\/p>\n<p>Director QA Compliance, Global Quality<\/p>\n<\/div>\n<div id=\"coloplast-yildiran-handan\" class=\"modal fade speaker-modal speaker-modal--light\" tabindex=\"-1\">\n<div class=\"modal-dialog modal-lg modal-dialog-scrollable\">\n<div class=\"modal-content\">\n<div class=\"modal-body\">\n                <button type=\"button\" class=\"modal-btn-close\" data-bs-dismiss=\"modal\" aria-label=\"Close\"><br \/>\n                    <span class=\"icon ready\" data-icon=\"close\" style=\"--icon: url('/medtech/wp-json/wp/v2/pages/65999/wp-content/themes/veeva2015/assets/svg/icons/close.svg');\"><\/span><br \/>\n                <\/button><\/p>\n<div class=\"modal-speaker-info\">\n<div class=\"avatar-thumbnail\">\n                        <img decoding=\"async\" src=\"https:\/\/www.veeva.com\/medtech\/wp-content\/uploads\/2026\/08\/Handan-Yildiran-600x390-1.png\" alt=\"\" \/>\n                    <\/div>\n<div class=\"modal-speaker-info__text\">\n<h5 class=\"speaker-name\">Handan Yildiran<\/h5>\n<p>\n                            <span class=\"speaker-company\">Coloplast<\/span><br \/>\n                            <span class=\"speaker-position\"> Director QA Compliance, Global Quality <\/span>\n                        <\/p>\n<\/p><\/div>\n<\/p><\/div>\n<hr class=\"modal-inner-separator\" \/>\n<div class=\"modal-speaker-bio\">\n<p>\n                        Handan governs global quality processes and digital systems, including the ³Ô¹Ï±¬ÁÏ Quality Platform, across the full product lifecycle. She joined Coloplast in 2014 and has held key leadership positions at both HQ and manufacturing sites, specializing in scaling quality capabilities that simplify compliance.\n                    <\/p>\n<\/p><\/div>\n<div class=\"modal-speaker-session\">\n<h5>Sessions<\/h5>\n<hr \/>\n<p>                    <a class=\"modal-speaker-session__item\" href=\"https:\/\/www.veeva.com\/medtech\/eu-summit-2026\/agenda\/#j-19\"><\/p>\n<h6>Coloplast: Maintaining Lean Quality Processes for Long-Term Success<\/h6>\n<p>11\/3\/2026 2:45 p.m.<\/p>\n<p>    <span class=\"forward-arrow\"><\/span><br \/>\n<\/a><\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/div>\n<div class=\"person-card-events person-card-events--light\" data-bs-toggle=\"modal\" data-bs-target=\"#cytiva-racordon-pape-sandra\">\n    <img decoding=\"async\" class=\"person-card-events__thumbnail\" src=\"https:\/\/www.veeva.com\/medtech\/wp-content\/uploads\/2026\/08\/Image-4.png\" alt=\"\" \/><\/p>\n<h6>Sandra Racordon-Pape<\/h6>\n<p class=\"person-card-events__company\">Cytiva<\/p>\n<p>Director Regulatory Science and Strategy<\/p>\n<\/div>\n<div id=\"cytiva-racordon-pape-sandra\" class=\"modal fade speaker-modal speaker-modal--light\" tabindex=\"-1\">\n<div class=\"modal-dialog modal-lg modal-dialog-scrollable\">\n<div class=\"modal-content\">\n<div class=\"modal-body\">\n                <button type=\"button\" class=\"modal-btn-close\" data-bs-dismiss=\"modal\" aria-label=\"Close\"><br \/>\n                    <span class=\"icon ready\" data-icon=\"close\" style=\"--icon: url('/medtech/wp-json/wp/v2/pages/65999/wp-content/themes/veeva2015/assets/svg/icons/close.svg');\"><\/span><br \/>\n                <\/button><\/p>\n<div class=\"modal-speaker-info\">\n<div class=\"avatar-thumbnail\">\n                        <img decoding=\"async\" src=\"https:\/\/www.veeva.com\/medtech\/wp-content\/uploads\/2026\/08\/Image-4.png\" alt=\"\" \/>\n                    <\/div>\n<div class=\"modal-speaker-info__text\">\n<h5 class=\"speaker-name\">Sandra Racordon-Pape<\/h5>\n<p>\n                            <span class=\"speaker-company\">Cytiva<\/span><br \/>\n                            <span class=\"speaker-position\"> Director Regulatory Science and Strategy <\/span>\n                        <\/p>\n<\/p><\/div>\n<\/p><\/div>\n<hr class=\"modal-inner-separator\" \/>\n<div class=\"modal-speaker-bio\">\n<p>\n                        Sandra leads initiatives in regulatory intelligence, digital transformation, and CMC strategy at Cytiva. She brings over 25 years of experience in QA\/RA and specializes in global regulatory frameworks and digital enablement like ³Ô¹Ï±¬ÁÏ RIM to accelerate submissions and drive compliant, data-driven ecosystems.\n                    <\/p>\n<\/p><\/div>\n<div class=\"modal-speaker-session\">\n<h5>Sessions<\/h5>\n<hr \/>\n<p>                    <a class=\"modal-speaker-session__item\" href=\"https:\/\/www.veeva.com\/medtech\/eu-summit-2026\/agenda\/#j-8\"><\/p>\n<h6>Cytiva: Solving Change Management Friction in Multi-Year Regulatory Transformations<br \/>\n<\/h6>\n<p>11\/3\/2026 11:30 a.m.<\/p>\n<p>    <span class=\"forward-arrow\"><\/span><br \/>\n<\/a><\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/div>\n<div class=\"person-card-events person-card-events--light\" data-bs-toggle=\"modal\" data-bs-target=\"#dexcom--avery-blake\">\n    <img decoding=\"async\" class=\"person-card-events__thumbnail\" src=\"https:\/\/www.veeva.com\/medtech\/wp-content\/uploads\/2026\/08\/Image-42.png\" alt=\"\" \/><\/p>\n<h6>Blake Avery<\/h6>\n<p class=\"person-card-events__company\">Dexcom <\/p>\n<p>Director, Commercial Excellence, EMEA<\/p>\n<\/div>\n<div id=\"dexcom--avery-blake\" class=\"modal fade speaker-modal speaker-modal--light\" tabindex=\"-1\">\n<div class=\"modal-dialog modal-lg modal-dialog-scrollable\">\n<div class=\"modal-content\">\n<div class=\"modal-body\">\n                <button type=\"button\" class=\"modal-btn-close\" data-bs-dismiss=\"modal\" aria-label=\"Close\"><br \/>\n                    <span class=\"icon ready\" data-icon=\"close\" style=\"--icon: url('/medtech/wp-json/wp/v2/pages/65999/wp-content/themes/veeva2015/assets/svg/icons/close.svg');\"><\/span><br \/>\n                <\/button><\/p>\n<div class=\"modal-speaker-info\">\n<div class=\"avatar-thumbnail\">\n                        <img decoding=\"async\" src=\"https:\/\/www.veeva.com\/medtech\/wp-content\/uploads\/2026\/08\/Image-42.png\" alt=\"\" \/>\n                    <\/div>\n<div class=\"modal-speaker-info__text\">\n<h5 class=\"speaker-name\">Blake Avery<\/h5>\n<p>\n                            <span class=\"speaker-company\">Dexcom <\/span><br \/>\n                            <span class=\"speaker-position\"> Director, Commercial Excellence, EMEA <\/span>\n                        <\/p>\n<\/p><\/div>\n<\/p><\/div>\n<hr class=\"modal-inner-separator\" \/>\n<div class=\"modal-speaker-bio\">\n<p>\n                        Blake leads strategic commercial initiatives across CRM transformation, data management, customer engagement, and field enablement EMEA. By aligning business strategy with technology, he focuses on balancing rapid value delivery with long-term capability building to drive measurable growth. Previously, Blake led commercial strategy and technology initiatives for medtech organizations at ZS.\n                    <\/p>\n<\/p><\/div>\n<div class=\"modal-speaker-session\">\n<h5>Sessions<\/h5>\n<hr \/>\n<p>                    <a class=\"modal-speaker-session__item\" href=\"https:\/\/www.veeva.com\/medtech\/eu-summit-2026\/agenda\/#j-10\"><\/p>\n<h6>Dexcom: Turn Data into Predictive Field Intelligence<\/h6>\n<p>11\/3\/2026 11:30 a.m.<\/p>\n<p>    <span class=\"forward-arrow\"><\/span><br \/>\n<\/a><\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/div>\n<div class=\"person-card-events person-card-events--light\" data-bs-toggle=\"modal\" data-bs-target=\"#dnv-product-assurance-as-shiryaev-alexey\">\n    <img decoding=\"async\" class=\"person-card-events__thumbnail\" src=\"https:\/\/www.veeva.com\/medtech\/wp-content\/uploads\/2026\/08\/Image-19.png\" alt=\"\" \/><\/p>\n<h6>Alexey Shiryaev<\/h6>\n<p class=\"person-card-events__company\">DNV Product Assurance AS<\/p>\n<p>Director of Certification<\/p>\n<\/div>\n<div id=\"dnv-product-assurance-as-shiryaev-alexey\" class=\"modal fade speaker-modal speaker-modal--light\" tabindex=\"-1\">\n<div class=\"modal-dialog modal-lg modal-dialog-scrollable\">\n<div class=\"modal-content\">\n<div class=\"modal-body\">\n                <button type=\"button\" class=\"modal-btn-close\" data-bs-dismiss=\"modal\" aria-label=\"Close\"><br \/>\n                    <span class=\"icon ready\" data-icon=\"close\" style=\"--icon: url('/medtech/wp-json/wp/v2/pages/65999/wp-content/themes/veeva2015/assets/svg/icons/close.svg');\"><\/span><br \/>\n                <\/button><\/p>\n<div class=\"modal-speaker-info\">\n<div class=\"avatar-thumbnail\">\n                        <img decoding=\"async\" src=\"https:\/\/www.veeva.com\/medtech\/wp-content\/uploads\/2026\/08\/Image-19.png\" alt=\"\" \/>\n                    <\/div>\n<div class=\"modal-speaker-info__text\">\n<h5 class=\"speaker-name\">Alexey Shiryaev<\/h5>\n<p>\n                            <span class=\"speaker-company\">DNV Product Assurance AS<\/span><br \/>\n                            <span class=\"speaker-position\"> Director of Certification <\/span>\n                        <\/p>\n<\/p><\/div>\n<\/p><\/div>\n<hr class=\"modal-inner-separator\" \/>\n<div class=\"modal-speaker-bio\">\n<p>\n                        Alongside his role at DNV Product Assurance, Alex serves as President of Team-NB, the European Association of Notified Bodies for medical devices. He brings over 13 years of notified body experience, building on his previous career in medical research and pediatric surgery.\n                    <\/p>\n<\/p><\/div>\n<div class=\"modal-speaker-session\">\n<h5>Sessions<\/h5>\n<hr \/>\n<p>                    <a class=\"modal-speaker-session__item\" href=\"https:\/\/www.veeva.com\/medtech\/eu-summit-2026\/agenda\/#j-3\"><\/p>\n<h6>BSI, DNV Product Assurance, and MHRA: Continuous Compliance in a Rapidly Changing Regulatory Landscape<\/h6>\n<p>11\/3\/2026 9:45 a.m.<\/p>\n<p>    <span class=\"forward-arrow\"><\/span><br \/>\n<\/a><\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/div>\n<div class=\"person-card-events person-card-events--light\" data-bs-toggle=\"modal\" data-bs-target=\"#gmed-patten-tom\">\n    <img decoding=\"async\" class=\"person-card-events__thumbnail\" src=\"https:\/\/www.veeva.com\/medtech\/wp-content\/uploads\/2026\/08\/Image-9.png\" alt=\"\" \/><\/p>\n<h6>Tom Patten<\/h6>\n<p class=\"person-card-events__company\">GMED<\/p>\n<p>IVDR International Manager<\/p>\n<\/div>\n<div id=\"gmed-patten-tom\" class=\"modal fade speaker-modal speaker-modal--light\" tabindex=\"-1\">\n<div class=\"modal-dialog modal-lg modal-dialog-scrollable\">\n<div class=\"modal-content\">\n<div class=\"modal-body\">\n                <button type=\"button\" class=\"modal-btn-close\" data-bs-dismiss=\"modal\" aria-label=\"Close\"><br \/>\n                    <span class=\"icon ready\" data-icon=\"close\" style=\"--icon: url('/medtech/wp-json/wp/v2/pages/65999/wp-content/themes/veeva2015/assets/svg/icons/close.svg');\"><\/span><br \/>\n                <\/button><\/p>\n<div class=\"modal-speaker-info\">\n<div class=\"avatar-thumbnail\">\n                        <img decoding=\"async\" src=\"https:\/\/www.veeva.com\/medtech\/wp-content\/uploads\/2026\/08\/Image-9.png\" alt=\"\" \/>\n                    <\/div>\n<div class=\"modal-speaker-info__text\">\n<h5 class=\"speaker-name\">Tom Patten<\/h5>\n<p>\n                            <span class=\"speaker-company\">GMED<\/span><br \/>\n                            <span class=\"speaker-position\"> IVDR International Manager <\/span>\n                        <\/p>\n<\/p><\/div>\n<\/p><\/div>\n<hr class=\"modal-inner-separator\" \/>\n<div class=\"modal-speaker-bio\">\n<p>\n                        With more than 13 years in the IVD industry, Tom now serves as IVDR\/IVD International Manager at GMED and Secretary of the NBCG-Med executive committee. His background includes over 5 years of notified body experience, featuring multiple leadership roles.\n                    <\/p>\n<\/p><\/div>\n<div class=\"modal-speaker-session\">\n<h5>Sessions<\/h5>\n<hr \/>\n<p>                    <a class=\"modal-speaker-session__item\" href=\"https:\/\/www.veeva.com\/medtech\/eu-summit-2026\/agenda\/#j-31\"><\/p>\n<h6>ABHI and GMED: 10 Essentials for a Simplified Digital Regulatory Future<\/h6>\n<p>11\/4\/2026 9:00 a.m.<\/p>\n<p>    <span class=\"forward-arrow\"><\/span><br \/>\n<\/a><\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/div>\n<div class=\"person-card-events person-card-events--light\" data-bs-toggle=\"modal\" data-bs-target=\"#medtronic-brasher-d-rebecca\">\n    <img decoding=\"async\" class=\"person-card-events__thumbnail\" src=\"https:\/\/www.veeva.com\/medtech\/wp-content\/uploads\/2026\/09\/Image-1.png\" alt=\"\" \/><\/p>\n<h6>Rebecca D. Brasher<\/h6>\n<p class=\"person-card-events__company\">Medtronic<\/p>\n<p>Regulatory Affairs Director- Ad Promo and Regulatory Labeling<\/p>\n<\/div>\n<div id=\"medtronic-brasher-d-rebecca\" class=\"modal fade speaker-modal speaker-modal--light\" tabindex=\"-1\">\n<div class=\"modal-dialog modal-lg modal-dialog-scrollable\">\n<div class=\"modal-content\">\n<div class=\"modal-body\">\n                <button type=\"button\" class=\"modal-btn-close\" data-bs-dismiss=\"modal\" aria-label=\"Close\"><br \/>\n                    <span class=\"icon ready\" data-icon=\"close\" style=\"--icon: url('/medtech/wp-json/wp/v2/pages/65999/wp-content/themes/veeva2015/assets/svg/icons/close.svg');\"><\/span><br \/>\n                <\/button><\/p>\n<div class=\"modal-speaker-info\">\n<div class=\"avatar-thumbnail\">\n                        <img decoding=\"async\" src=\"https:\/\/www.veeva.com\/medtech\/wp-content\/uploads\/2026\/09\/Image-1.png\" alt=\"\" \/>\n                    <\/div>\n<div class=\"modal-speaker-info__text\">\n<h5 class=\"speaker-name\">Rebecca D. Brasher<\/h5>\n<p>\n                            <span class=\"speaker-company\">Medtronic<\/span><br \/>\n                            <span class=\"speaker-position\"> Regulatory Affairs Director- Ad Promo and Regulatory Labeling <\/span>\n                        <\/p>\n<\/p><\/div>\n<\/p><\/div>\n<hr class=\"modal-inner-separator\" \/>\n<div class=\"modal-speaker-bio\">\n<p>\n                        Becki leads regulatory affairs initiatives for advertising and promotion at Medtronic. She also focuses on modernizing promotional review workflows and scaling digital solutions across highly regulated environments.\n                    <\/p>\n<\/p><\/div>\n<div class=\"modal-speaker-session\">\n<h5>Sessions<\/h5>\n<hr \/>\n<p>                    <a class=\"modal-speaker-session__item\" href=\"https:\/\/www.veeva.com\/medtech\/eu-summit-2026\/agenda\/#j-4\"><\/p>\n<h6>Medtronic: Vault AI for Next-Gen Promotions<\/h6>\n<p>11\/3\/2026 9:45 a.m.<\/p>\n<p>    <span class=\"forward-arrow\"><\/span><br \/>\n<\/a><\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/div>\n<div class=\"person-card-events person-card-events--light\" data-bs-toggle=\"modal\" data-bs-target=\"#mhra-reid-rob\">\n    <img decoding=\"async\" class=\"person-card-events__thumbnail\" src=\"https:\/\/www.veeva.com\/medtech\/wp-content\/uploads\/2026\/08\/Image-18.png\" alt=\"\" \/><\/p>\n<h6>Rob Reid<\/h6>\n<p class=\"person-card-events__company\">MHRA<\/p>\n<p>Deputy Director, Innovative Devices<\/p>\n<\/div>\n<div id=\"mhra-reid-rob\" class=\"modal fade speaker-modal speaker-modal--light\" tabindex=\"-1\">\n<div class=\"modal-dialog modal-lg modal-dialog-scrollable\">\n<div class=\"modal-content\">\n<div class=\"modal-body\">\n                <button type=\"button\" class=\"modal-btn-close\" data-bs-dismiss=\"modal\" aria-label=\"Close\"><br \/>\n                    <span class=\"icon ready\" data-icon=\"close\" style=\"--icon: url('/medtech/wp-json/wp/v2/pages/65999/wp-content/themes/veeva2015/assets/svg/icons/close.svg');\"><\/span><br \/>\n                <\/button><\/p>\n<div class=\"modal-speaker-info\">\n<div class=\"avatar-thumbnail\">\n                        <img decoding=\"async\" src=\"https:\/\/www.veeva.com\/medtech\/wp-content\/uploads\/2026\/08\/Image-18.png\" alt=\"\" \/>\n                    <\/div>\n<div class=\"modal-speaker-info__text\">\n<h5 class=\"speaker-name\">Rob Reid<\/h5>\n<p>\n                            <span class=\"speaker-company\">MHRA<\/span><br \/>\n                            <span class=\"speaker-position\"> Deputy Director, Innovative Devices <\/span>\n                        <\/p>\n<\/p><\/div>\n<\/p><\/div>\n<hr class=\"modal-inner-separator\" \/>\n<div class=\"modal-speaker-bio\">\n<p>\n                        Rob leads the MHRA\u2019s innovative devices team, driving the reform of the UK\u2019s medical device regulations as deputy director. He draws on five years of regulatory policy experience at the office for life sciences and a background leading the national physical laboratory\u2019s biometrology group.\n                    <\/p>\n<\/p><\/div>\n<div class=\"modal-speaker-session\">\n<h5>Sessions<\/h5>\n<hr \/>\n<p>                    <a class=\"modal-speaker-session__item\" href=\"https:\/\/www.veeva.com\/medtech\/eu-summit-2026\/agenda\/#j-3\"><\/p>\n<h6>BSI, DNV Product Assurance, and MHRA: Continuous Compliance in a Rapidly Changing Regulatory Landscape<\/h6>\n<p>11\/3\/2026 9:45 a.m.<\/p>\n<p>    <span class=\"forward-arrow\"><\/span><br \/>\n<\/a><\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/div>\n<div class=\"person-card-events person-card-events--light\" data-bs-toggle=\"modal\" data-bs-target=\"#novocure-banta-brian\">\n    <img decoding=\"async\" class=\"person-card-events__thumbnail\" src=\"https:\/\/www.veeva.com\/medtech\/wp-content\/uploads\/2026\/08\/Image-24.png\" alt=\"\" \/><\/p>\n<h6>Brian Banta<\/h6>\n<p class=\"person-card-events__company\">Novocure<\/p>\n<p>Senior Manager, Business Process Engineering<\/p>\n<\/div>\n<div id=\"novocure-banta-brian\" class=\"modal fade speaker-modal speaker-modal--light\" tabindex=\"-1\">\n<div class=\"modal-dialog modal-lg modal-dialog-scrollable\">\n<div class=\"modal-content\">\n<div class=\"modal-body\">\n                <button type=\"button\" class=\"modal-btn-close\" data-bs-dismiss=\"modal\" aria-label=\"Close\"><br \/>\n                    <span class=\"icon ready\" data-icon=\"close\" style=\"--icon: url('/medtech/wp-json/wp/v2/pages/65999/wp-content/themes/veeva2015/assets/svg/icons/close.svg');\"><\/span><br \/>\n                <\/button><\/p>\n<div class=\"modal-speaker-info\">\n<div class=\"avatar-thumbnail\">\n                        <img decoding=\"async\" src=\"https:\/\/www.veeva.com\/medtech\/wp-content\/uploads\/2026\/08\/Image-24.png\" alt=\"\" \/>\n                    <\/div>\n<div class=\"modal-speaker-info__text\">\n<h5 class=\"speaker-name\">Brian Banta<\/h5>\n<p>\n                            <span class=\"speaker-company\">Novocure<\/span><br \/>\n                            <span class=\"speaker-position\"> Senior Manager, Business Process Engineering <\/span>\n                        <\/p>\n<\/p><\/div>\n<\/p><\/div>\n<hr class=\"modal-inner-separator\" \/>\n<div class=\"modal-speaker-bio\">\n<p>\n                        Brian modernizes global operations at Novocure across clinical, safety, supply chain, quality, and regulatory. He specializes in platform-based strategies that reduce complexity, scale workflows, and align technology solutions with broader business goals.\n                    <\/p>\n<\/p><\/div>\n<div class=\"modal-speaker-session\">\n<h5>Sessions<\/h5>\n<hr \/>\n<p>                    <a class=\"modal-speaker-session__item\" href=\"https:\/\/www.veeva.com\/medtech\/eu-summit-2026\/agenda\/#j-36\"><\/p>\n<h6>Novocure: Standardize vs. Customize for Clean, AI-Ready RIM Architecture <\/h6>\n<p>11\/4\/2026 10:00 a.m.<\/p>\n<p>    <span class=\"forward-arrow\"><\/span><br \/>\n<\/a><\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/div>\n<div class=\"person-card-events person-card-events--light\" data-bs-toggle=\"modal\" data-bs-target=\"#philips-brunner-jos\">\n    <img decoding=\"async\" class=\"person-card-events__thumbnail\" src=\"https:\/\/www.veeva.com\/medtech\/wp-content\/uploads\/2026\/08\/Image-6.png\" alt=\"\" \/><\/p>\n<h6>Jos Brunner<\/h6>\n<p class=\"person-card-events__company\">Philips<\/p>\n<p>Claims Program Manager<\/p>\n<\/div>\n<div id=\"philips-brunner-jos\" class=\"modal fade speaker-modal speaker-modal--light\" tabindex=\"-1\">\n<div class=\"modal-dialog modal-lg modal-dialog-scrollable\">\n<div class=\"modal-content\">\n<div class=\"modal-body\">\n                <button type=\"button\" class=\"modal-btn-close\" data-bs-dismiss=\"modal\" aria-label=\"Close\"><br \/>\n                    <span class=\"icon ready\" data-icon=\"close\" style=\"--icon: url('/medtech/wp-json/wp/v2/pages/65999/wp-content/themes/veeva2015/assets/svg/icons/close.svg');\"><\/span><br \/>\n                <\/button><\/p>\n<div class=\"modal-speaker-info\">\n<div class=\"avatar-thumbnail\">\n                        <img decoding=\"async\" src=\"https:\/\/www.veeva.com\/medtech\/wp-content\/uploads\/2026\/08\/Image-6.png\" alt=\"\" \/>\n                    <\/div>\n<div class=\"modal-speaker-info__text\">\n<h5 class=\"speaker-name\">Jos Brunner<\/h5>\n<p>\n                            <span class=\"speaker-company\">Philips<\/span><br \/>\n                            <span class=\"speaker-position\"> Claims Program Manager <\/span>\n                        <\/p>\n<\/p><\/div>\n<\/p><\/div>\n<hr class=\"modal-inner-separator\" \/>\n<div class=\"modal-speaker-bio\">\n<p>\n                        Jos leads the claims program at Philips, driving the enterprise deployment of ³Ô¹Ï±¬ÁÏ PromoMats. Leveraging his medtech innovation background, he collaborates across commercial, regulatory, and IT functions to scale compliant, AI-enabled content and global localization.\n                    <\/p>\n<\/p><\/div>\n<div class=\"modal-speaker-session\">\n<h5>Sessions<\/h5>\n<hr \/>\n<p>                    <a class=\"modal-speaker-session__item\" href=\"https:\/\/www.veeva.com\/medtech\/eu-summit-2026\/agenda\/#j-15\"><\/p>\n<h6>Philips: Modernizing Claims Management for Global Scale<\/h6>\n<p>11\/3\/2026 12:30 p.m.<\/p>\n<p>    <span class=\"forward-arrow\"><\/span><br \/>\n<\/a><\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/div>\n<div class=\"person-card-events person-card-events--light\" data-bs-toggle=\"modal\" data-bs-target=\"#smithnephew-pttker-markus\">\n    <img decoding=\"async\" class=\"person-card-events__thumbnail\" src=\"https:\/\/www.veeva.com\/medtech\/wp-content\/uploads\/2026\/08\/Image-33.png\" alt=\"\" \/><\/p>\n<h6>Markus P\u00f6ttker<\/h6>\n<p class=\"person-card-events__company\">Smith+Nephew<\/p>\n<p>Director, Global Post-Market Surveillance<\/p>\n<\/div>\n<div id=\"smithnephew-pttker-markus\" class=\"modal fade speaker-modal speaker-modal--light\" tabindex=\"-1\">\n<div class=\"modal-dialog modal-lg modal-dialog-scrollable\">\n<div class=\"modal-content\">\n<div class=\"modal-body\">\n                <button type=\"button\" class=\"modal-btn-close\" data-bs-dismiss=\"modal\" aria-label=\"Close\"><br \/>\n                    <span class=\"icon ready\" data-icon=\"close\" style=\"--icon: url('/medtech/wp-json/wp/v2/pages/65999/wp-content/themes/veeva2015/assets/svg/icons/close.svg');\"><\/span><br \/>\n                <\/button><\/p>\n<div class=\"modal-speaker-info\">\n<div class=\"avatar-thumbnail\">\n                        <img decoding=\"async\" src=\"https:\/\/www.veeva.com\/medtech\/wp-content\/uploads\/2026\/08\/Image-33.png\" alt=\"\" \/>\n                    <\/div>\n<div class=\"modal-speaker-info__text\">\n<h5 class=\"speaker-name\">Markus P\u00f6ttker<\/h5>\n<p>\n                            <span class=\"speaker-company\">Smith+Nephew<\/span><br \/>\n                            <span class=\"speaker-position\"> Director, Global Post-Market Surveillance <\/span>\n                        <\/p>\n<\/p><\/div>\n<\/p><\/div>\n<hr class=\"modal-inner-separator\" \/>\n<div class=\"modal-speaker-bio\">\n<p>\n                        With 15 years of quality and regulatory experience, Markus is an expert in data-driven post-market surveillance and European regulatory compliance. He chairs MedTech Europe\u2019s PMS &#038; vigilance working group, contributes to MDCG task forces, and is a recipient of the 2026 RAPS 50for50 regulatory trailblazer award.\n                    <\/p>\n<\/p><\/div>\n<div class=\"modal-speaker-session\">\n<h5>Sessions<\/h5>\n<hr \/>\n<p>                    <a class=\"modal-speaker-session__item\" href=\"https:\/\/www.veeva.com\/medtech\/eu-summit-2026\/agenda\/#j-37\"><\/p>\n<h6>Smith+Nephew and Tosoh: Evaluating the Impact of Risk-Based Decisions on Quality Innovation<\/h6>\n<p>11\/4\/2026 10:00 a.m.<\/p>\n<p>    <span class=\"forward-arrow\"><\/span><br \/>\n<\/a><\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/div>\n<div class=\"person-card-events person-card-events--light\" data-bs-toggle=\"modal\" data-bs-target=\"#teleflex-mcdonald-john\">\n    <img decoding=\"async\" class=\"person-card-events__thumbnail\" src=\"https:\/\/www.veeva.com\/medtech\/wp-content\/uploads\/2026\/08\/Image-10.png\" alt=\"\" \/><\/p>\n<h6>John McDonald<\/h6>\n<p class=\"person-card-events__company\">Teleflex<\/p>\n<p>Senior Director Clinical Evidence Generation<\/p>\n<\/div>\n<div id=\"teleflex-mcdonald-john\" class=\"modal fade speaker-modal speaker-modal--light\" tabindex=\"-1\">\n<div class=\"modal-dialog modal-lg modal-dialog-scrollable\">\n<div class=\"modal-content\">\n<div class=\"modal-body\">\n                <button type=\"button\" class=\"modal-btn-close\" data-bs-dismiss=\"modal\" aria-label=\"Close\"><br \/>\n                    <span class=\"icon ready\" data-icon=\"close\" style=\"--icon: url('/medtech/wp-json/wp/v2/pages/65999/wp-content/themes/veeva2015/assets/svg/icons/close.svg');\"><\/span><br \/>\n                <\/button><\/p>\n<div class=\"modal-speaker-info\">\n<div class=\"avatar-thumbnail\">\n                        <img decoding=\"async\" src=\"https:\/\/www.veeva.com\/medtech\/wp-content\/uploads\/2026\/08\/Image-10.png\" alt=\"\" \/>\n                    <\/div>\n<div class=\"modal-speaker-info__text\">\n<h5 class=\"speaker-name\">John McDonald<\/h5>\n<p>\n                            <span class=\"speaker-company\">Teleflex<\/span><br \/>\n                            <span class=\"speaker-position\"> Senior Director Clinical Evidence Generation <\/span>\n                        <\/p>\n<\/p><\/div>\n<\/p><\/div>\n<hr class=\"modal-inner-separator\" \/>\n<div class=\"modal-speaker-bio\">\n<p>\n                        With 20 years of medtech experience, John leads global clinical evidence generation at Teleflex. He specializes in international clinical programs and RWE for FDA\/MDR approvals, combining scientific rigor with a strategic mindset to drive global market adoption.\n                    <\/p>\n<\/p><\/div>\n<div class=\"modal-speaker-session\">\n<h5>Sessions<\/h5>\n<hr \/>\n<p>                    <a class=\"modal-speaker-session__item\" href=\"https:\/\/www.veeva.com\/medtech\/eu-summit-2026\/agenda\/#j-2\"><\/p>\n<h6>BSI and Teleflex: Leveraging Clinical Evidence and RWD to Accelerate Market Access<\/h6>\n<p>11\/3\/2026 9:45 a.m.<\/p>\n<p>    <span class=\"forward-arrow\"><\/span><br \/>\n<\/a><\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/div>\n<div class=\"person-card-events person-card-events--light\" data-bs-toggle=\"modal\" data-bs-target=\"#terumo-europe-nv-verhaert-koen\">\n    <img decoding=\"async\" class=\"person-card-events__thumbnail\" src=\"https:\/\/www.veeva.com\/medtech\/wp-content\/uploads\/2026\/08\/Image-41.png\" alt=\"\" \/><\/p>\n<h6>Koen Verhaert<\/h6>\n<p class=\"person-card-events__company\">Terumo Europe N.V.<\/p>\n<p>Vice President Quality, Regulatory &#038; Vigilance<\/p>\n<\/div>\n<div id=\"terumo-europe-nv-verhaert-koen\" class=\"modal fade speaker-modal speaker-modal--light\" tabindex=\"-1\">\n<div class=\"modal-dialog modal-lg modal-dialog-scrollable\">\n<div class=\"modal-content\">\n<div class=\"modal-body\">\n                <button type=\"button\" class=\"modal-btn-close\" data-bs-dismiss=\"modal\" aria-label=\"Close\"><br \/>\n                    <span class=\"icon ready\" data-icon=\"close\" style=\"--icon: url('/medtech/wp-json/wp/v2/pages/65999/wp-content/themes/veeva2015/assets/svg/icons/close.svg');\"><\/span><br \/>\n                <\/button><\/p>\n<div class=\"modal-speaker-info\">\n<div class=\"avatar-thumbnail\">\n                        <img decoding=\"async\" src=\"https:\/\/www.veeva.com\/medtech\/wp-content\/uploads\/2026\/08\/Image-41.png\" alt=\"\" \/>\n                    <\/div>\n<div class=\"modal-speaker-info__text\">\n<h5 class=\"speaker-name\">Koen Verhaert<\/h5>\n<p>\n                            <span class=\"speaker-company\">Terumo Europe N.V.<\/span><br \/>\n                            <span class=\"speaker-position\"> Vice President Quality, Regulatory &#038; Vigilance <\/span>\n                        <\/p>\n<\/p><\/div>\n<\/p><\/div>\n<hr class=\"modal-inner-separator\" \/>\n<div class=\"modal-speaker-bio\">\n<p>\n                        With over 25 years of quality and regulatory experience, Koen manages medical device and CDMO plants, driving operational excellence through practical, compliant, and locally adaptable processes. As a bio-engineer, he bridges global standards with local site needs to empower high-performing, cross-functional teams.\n                    <\/p>\n<\/p><\/div>\n<div class=\"modal-speaker-session\">\n<h5>Sessions<\/h5>\n<hr \/>\n<p>                    <a class=\"modal-speaker-session__item\" href=\"https:\/\/www.veeva.com\/medtech\/eu-summit-2026\/agenda\/#j-9\"><\/p>\n<h6>Terumo: Driving Quality Transformations with Fit-for-Purpose Quality Systems<\/h6>\n<p>11\/3\/2026 11:30 a.m.<\/p>\n<p>    <span class=\"forward-arrow\"><\/span><br \/>\n<\/a><\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/div>\n<div class=\"person-card-events person-card-events--light\" data-bs-toggle=\"modal\" data-bs-target=\"#tosoh-corporation-durso-emiliano\">\n    <img decoding=\"async\" class=\"person-card-events__thumbnail\" src=\"https:\/\/www.veeva.com\/medtech\/wp-content\/uploads\/2026\/08\/Image-17.png\" alt=\"\" \/><\/p>\n<h6>Emiliano D&#8217;Urso<\/h6>\n<p class=\"person-card-events__company\">Tosoh Corporation<\/p>\n<p>PMS &#038; Regulatory Intelligence Manager EMEA<\/p>\n<\/div>\n<div id=\"tosoh-corporation-durso-emiliano\" class=\"modal fade speaker-modal speaker-modal--light\" tabindex=\"-1\">\n<div class=\"modal-dialog modal-lg modal-dialog-scrollable\">\n<div class=\"modal-content\">\n<div class=\"modal-body\">\n                <button type=\"button\" class=\"modal-btn-close\" data-bs-dismiss=\"modal\" aria-label=\"Close\"><br \/>\n                    <span class=\"icon ready\" data-icon=\"close\" style=\"--icon: url('/medtech/wp-json/wp/v2/pages/65999/wp-content/themes/veeva2015/assets/svg/icons/close.svg');\"><\/span><br \/>\n                <\/button><\/p>\n<div class=\"modal-speaker-info\">\n<div class=\"avatar-thumbnail\">\n                        <img decoding=\"async\" src=\"https:\/\/www.veeva.com\/medtech\/wp-content\/uploads\/2026\/08\/Image-17.png\" alt=\"\" \/>\n                    <\/div>\n<div class=\"modal-speaker-info__text\">\n<h5 class=\"speaker-name\">Emiliano D&#8217;Urso<\/h5>\n<p>\n                            <span class=\"speaker-company\">Tosoh Corporation<\/span><br \/>\n                            <span class=\"speaker-position\"> PMS &#038; Regulatory Intelligence Manager EMEA <\/span>\n                        <\/p>\n<\/p><\/div>\n<\/p><\/div>\n<hr class=\"modal-inner-separator\" \/>\n<div class=\"modal-speaker-bio\">\n<p>\n                        Emiliano leads post-market surveillance strategy, vigilance, and IVDR regulatory intelligence at Tosoh Bioscience \u2013 Diagnostics EMEA. He also chairs MedTech Europe\u2019s IVD PMS &#038; vigilance working group, drawing on deep expertise in PMS, PSURs, EUDAMED readiness, and QMS integration to align regulators, notified bodies, and industry on practical EU compliance.\n                    <\/p>\n<\/p><\/div>\n<div class=\"modal-speaker-session\">\n<h5>Sessions<\/h5>\n<hr \/>\n<p>                    <a class=\"modal-speaker-session__item\" href=\"https:\/\/www.veeva.com\/medtech\/eu-summit-2026\/agenda\/#j-37\"><\/p>\n<h6>Smith+Nephew and Tosoh: Evaluating the Impact of Risk-Based Decisions on Quality Innovation<\/h6>\n<p>11\/4\/2026 10:00 a.m.<\/p>\n<p>    <span class=\"forward-arrow\"><\/span><br \/>\n<\/a><\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/p><\/div>\n<\/div>\n\n\t<\/div>\n<\/section>\n<!-- Speakers End -->\n\n<\/div>\n\n\n","protected":false},"excerpt":{"rendered":"","protected":false},"author":26,"featured_media":66082,"parent":65994,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"templates\/template-summit-speakers-2025-v2.php","meta":{"_acf_changed":false,"footnotes":""},"class_list":["post-65999","page","type-page","status-publish","has-post-thumbnail","hentry"],"acf":[],"aioseo_notices":[],"aioseo_head":"\n\t\t<!-- All in One SEO Pro 5.0.1 - aioseo.com -->\n\t<meta name=\"description\" content=\"Connect with medical device leaders at MedTech Summit Europe 2026 in Amsterdam. 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