Top Speakers at the Medical Device Product Life Cycle Conference: October 8-9

Don’t miss our international conference designed to navigate the complexities of medical device regulations and standards. This is your chance to gain essential knowledge and insights from top industry leaders who will simplify complex processes and provide invaluable tools.

Why Attend?
Whether you’re a Quality or Regulatory specialist, involved in design and development, clinical/performance evaluations, post-market clinical follow-up, process development, or Quality Assurance/Regulatory Affairs, this conference is essential for staying ahead in your field.

What to Expect:
Our agenda covers key activities from both the pre- and post-market phases and features:

• Expert insights from industry leaders
• Legal perspectives and patient experiences
• Input from multiple Notified Bodies

Featured Speakers:

• Sharmila Gardner, Technical Documentation Manager & Head of UK Approved Body – Intertek Medical Notified Body
• Pontus Gedda, Medical Device Specialist – RISE Research Institutes of Sweden
• Anna Kuptel, Team Leader Site Auditor – TÜV SÜD
• Richard Holborow, Global Head Clinical Compliance – BSI
• Judith de Wilde, Attorney at Law – Axon Lawyers
• Sandra Larsson, Consultant & Life Science Industry Lead – TECHNIA
• Erik Hansson, Expert in Global Harmonisation of Medical Device Regulations
• Azadeh Hajipour, Senior Regulatory Consultant – GBA Key2Compliance
• Henrik Eriksson, Dialysis Patient from Njurförbundet
• Dr. Madlon Timme & Dr. Kristina Then – GBA Group Pharma & Medical Devices
• Cyrille Michaud, Managing Partner – MD101 Consulting

Learn more about our speakers and their presentations here. Explore the details to see how they will contribute to the conference and enhance your understanding of medical device innovation.

🚀 Seats are filling up fast! Register now to secure your spot and stay ahead in the evolving world of medical device innovation. 💡