{"id":7,"date":"2019-07-24T09:33:07","date_gmt":"2019-07-24T09:33:07","guid":{"rendered":"http:\/\/ecn2020.www.bioevents.net?page_id=7"},"modified":"2023-06-20T12:08:17","modified_gmt":"2023-06-20T12:08:17","slug":"home-2-2-2","status":"publish","type":"page","link":"https:\/\/eu-mdr2023.com\/","title":{"rendered":"home"},"content":{"rendered":"\t\t
The EU Medical Devices Conference<\/p>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
EU-MDR
How to Succeed?<\/p>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
Brussels, Belgium<\/p>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
It is our great pleasure to welcome you to the EU Medical Devices Conference \u2018EU-MDR \u2013 How to Succeed?\u2019<\/strong> that will take place 6 – 7 July 2023<\/strong> in Brussels, Belgium<\/strong>.<\/p> 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 on the optimal MDR strategy. We included speakers from Notified Bodies, device manufacturers and consultants to ensure participants will hear and interact with the relevant stakeholders.<\/p> The program of the upcoming conference covers topics from the development of a regulatory strategy to the clinical and post-market requirements for medical and combination devices in Europe. Globally leading experts in these fields will attend and the participants will benefit from the possibility of intensive exchange and collaboration during the hands-on workshops.<\/p> This conference will welcome participants who are working in the fields of regulatory requirements, clinical evaluation and post-market surveillance and who want to deepen their existing knowledge in hands-on workshops. We are looking forward to participants ranging from start-ups to global medical device companies.<\/p> 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 audience.<\/p> We look forward to meeting you at \u2018EU-MDR \u2013 How to Succeed?\u2019<\/strong> in Brussels.\u00a0<\/p>\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t Founder and CEO Akra Team, Germany Click here to view Participate in the View Industry
\u2022 Legal requirements and classification changes
\u2022 Planning the conformity assessment and compiling the Technical Documentation
\u2022 Collecting clinical evidence and compiling the Clinical Evaluation Report
\u2022 Planning and conducting the required PMS and PMCF activities<\/p>\n\t\t\t\t\t\t\tBassil Akra\t\t\t\t\t\t<\/h4>\n\t\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t
\nConference Chair<\/p>\n\t\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\t\t\tConference Program\t\t\t\t\t\t<\/h4>\n\t\t\t\t\t<\/a>\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t
our expert speakers<\/p>\n\t\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\tLearn More\t\t\t\t\t<\/a>\n\t\t\t\t\t\t\t<\/div>\n\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<\/div>\n\t\t\t\t\n\t\t\t\t\t\t\tWorkshops\t\t\t\t\t\t<\/h4>\n\t\t\t\t\t<\/a>\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t
\n4 interactive workshops<\/p>\n\t\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\tLearn More\t\t\t\t\t<\/a>\n\t\t\t\t\t\t\t<\/div>\n\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<\/div>\n\t\t\t\t\n\t\t\t\t\t\t\tIndustry Support\t\t\t\t\t\t<\/h4>\n\t\t\t\t\t<\/a>\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t
Opportunities<\/p>\n\t\t\t\t\t<\/div>\n\t\t\t\t\n\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\tLearn More\t\t\t\t\t<\/a>\n\t\t\t\t\t\t\t<\/div>\n\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<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\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\tRegister Now <\/h2>\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
EU-MDR<\/h2>\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