Don’t miss our international conference tailored to navigating the complexities of medical device regulations and standards.
Why Attend?
Gain invaluable knowledge from top industry leaders who will simplify complex processes and provide essential tools for success. Whether you’re in Quality, Regulatory, Design & Development, Clinical/Performance Evaluations, or Post-Market Surveillance, this conference is essential for staying ahead in the field.
What to Expect?
Our agenda covers both pre- and post-market phases, with sessions like:
• How to Cross the Atlantic: Adapting European Expertise for U.S. Regulatory Success
• Working with AI-based Products – How to Add ISO 42001 Compliance to Your ISO 13485 QMS
• What is Important to a Notified Body in the Post-Market Surveillance of a Device?
• Your MDR Technical Documentation Submission: Key Success Factors, Plus a Mistake to Avoid
• Harmonization of Medical Device Regulations – Current Initiatives by IMDRF
• Product Liability Throughout the Medical Device Supply Chain: A Changing Landscape