{"id":4315,"date":"2024-02-13T07:20:33","date_gmt":"2024-02-13T07:20:33","guid":{"rendered":"https:\/\/www.bioevents.net\/rmd2025\/?page_id=4315"},"modified":"2024-07-16T10:34:57","modified_gmt":"2024-07-16T10:34:57","slug":"dear-colleagues-new","status":"publish","type":"page","link":"https:\/\/rmd2025.com\/dear-colleagues-new\/","title":{"rendered":"Conference Chair Welcome"},"content":{"rendered":"\t\t
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Dear Colleagues,<\/span><\/span><\/div>
\u00a0<\/div>
It is with great pleasure that we extend our warm invitation to you to the <\/span>9th EAAR Annual Conference on Medical Device Regulations<\/strong>, a prestigious event proudly\u00a0<\/span>organized\u00a0by the European Association of Authorised Representatives\u00a0(EAAR)<\/strong>. This distinguished event is set to unfold against the backdrop of the elegant Sheraton Brussels Airport Hotel in Belgium, offering an educational experience on the\u00a0<\/span>24th-25th of February 2025<\/strong>.<\/span><\/span><\/div><\/div>

Our conference serves as an inclusive platform for all stakeholders across the medical and IVD medical devices landscape. With a dedicated focus on the challenges faced by manufacturers and other stakeholders in embracing the EU MDR and IVDR, the event holds promise for all attendees, irrespective of their diverse backgrounds. This occasion invites you to delve into the depths of European regulations, fostering insightful discussions on pivotal facets of these ever-evolving regulatory frameworks.<\/span><\/p>

Spanning topics from the divergence in national implementation of the regulations across Europe to cutting-edge regulatory topics concerning AI, clinical evaluation, UDI, post-market surveillance, and technical documentation, the Conference offers an all-encompassing journey. Covering the European Union, United Kingdom, and Switzerland, the Event is\u00a0poised\u00a0to unravel a myriad of subjects that are of paramount importance.<\/span><\/p>

The RMD Conference promises to be a momentous juncture for\u00a0combining\u00a0diverse actors and subjects within the compliance landscape. EU officials, Manufacturers, competent authorities, notified bodies, and business associations will converge, igniting a collective dialogue that holds the potential to shape the future of the industry.<\/span><\/p>

We look forward to meeting you at\u00a0RMD2025<\/strong>\u00a0in Brussels.<\/span><\/p>

Sincerely,<\/span><\/p>

\"\"<\/span><\/p>

Ludger\u00a0M\u00f6ller<\/strong><\/span><\/p>

EAAR Chairman, President, Medical Device Safety Service, Germany<\/em><\/span>
Conference Chair<\/em><\/span><\/p><\/div><\/div>\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>\n\t\t","protected":false},"excerpt":{"rendered":"

Dear Colleagues,\u00a0It is with great pleasure that we extend our warm invitation to you to the 9th EAAR Annual Conference on Medical Device Regulations, a prestigious event proudly\u00a0organized\u00a0by the European Association of Authorised Representatives\u00a0(EAAR). This distinguished event is set to unfold against the backdrop of the elegant Sheraton Brussels Airport Hotel in Belgium, offering an […]<\/p>\n","protected":false},"author":6,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"footnotes":""},"class_list":["post-4315","page","type-page","status-publish","hentry"],"acf":[],"yoast_head":"\nConference Chair Welcome - RMD2025<\/title>\n<meta name=\"description\" content=\"The 9th EAAR Annual Conference on Medical Device Regulations (RMD2025), which will take place 24-25 February 2025 in Brussels, Belgium.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/rmd2025.com\/dear-colleagues-new\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Conference Chair Welcome - 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