It is our great pleasure to welcome you to the EU Medical Devices Conference ‘EU-MDR – How to Succeed?’ 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 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.

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.

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.

The Conference will focus on the following key areas:
• Legal requirements and classification changes
• Planning the conformity assessment and compiling the Technical Documentation
• Collecting clinical evidence and compiling the Clinical Evaluation Report
• Planning and conducting the required PMS and PMCF activities

Join us also as a sponsor or exhibitor and benefit from maximum visibility and exposure to a broader audience.

We look forward to meeting you at ‘EU-MDR – How to Succeed?’ in Brussels.