{"id":370,"date":"2019-10-03T12:00:23","date_gmt":"2019-10-03T12:00:23","guid":{"rendered":"https:\/\/www.bioevents.net\/fibromyalgia2021\/?page_id=370"},"modified":"2023-04-18T13:42:04","modified_gmt":"2023-04-18T13:42:04","slug":"dear-colleague","status":"publish","type":"page","link":"https:\/\/eu-mdr2023.com\/dear-colleague\/","title":{"rendered":"Dear Colleagues,"},"content":{"rendered":"
It is our great pleasure to welcome you to the EU Medical Devices Conference \u2018EU-MDR \u2013 How to <\/strong> We will bring together international leaders in the field of the Medical Device Regulation (EU MDR) to The program of the upcoming conference covers topics from the development of a regulatory strategy This conference will welcome participants who are working in the fields of regulatory requirements, The Conference will focus on the following key areas: Join us also as a Sponsor or Exhibitor and benefit from maximum visibility and exposure to a broader We look forward to meeting you at \u2018EU-MDR \u2013 How to Succeed?\u2019<\/strong> in Brussels.<\/p>\n Sincerely,<\/p>\n <\/p>\n Bassil Akra It is our great pleasure to welcome you to the EU Medical Devices Conference \u2018EU-MDR \u2013 How to Succeed?\u2019 that will take place 6 – 7 July 2023 in Brussels, Belgium. We will bring together international leaders in the field of the Medical Device Regulation (EU MDR) to deliver talks and workshops that are idea-focused […]<\/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-370","page","type-page","status-publish","hentry"],"acf":[],"yoast_head":"\n
\nSucceed?<\/strong>\u2019 that will take place 6 – 7 July 2023<\/strong> in Brussels, Belgium<\/strong>.<\/p>\n
\ndeliver talks and workshops that are idea-focused on the optimal MDR strategy. We included speakers
\nfrom Notified Bodies, device manufacturers and consultants to ensure participants will hear and interact
\nwith the relevant stakeholders.<\/p>\n
\nto the clinical and post-market requirements for medical and combination devices in Europe. Globally
\nleading experts in these fields will attend and the participants will benefit from the possibility of
\nintensive exchange and collaboration during the hands-on workshops.<\/p>\n
\nclinical evaluation and post-market surveillance and who want to deepen their existing knowledge in
\nhands-on workshops. We are looking forward to participants ranging from start-ups to global medical
\ndevice companies.<\/p>\n
\n\u2022 Legal requirements and classification changes
\n\u2022 Planning the conformity assessment and compiling the Technical Documentation
\n\u2022 Collecting clinical evidence and compiling the Clinical Evaluation Report
\n\u2022 Planning and conducting the required PMS and PMCF activities<\/p>\n
\naudience.<\/p>\n
\n<\/strong>Founder and CEO Akra Team, Germany<\/em>
\nConference Chair<\/p>\n","protected":false},"excerpt":{"rendered":"