Don’t miss out on our upcoming Medical Device Product Life Cycle conference on October 8-9 in Stockholm, Sweden! Join us for an international event dedicated to navigating the complexities of medical device regulations and standards. Our speakers are industry leaders ready to equip you with essential knowledge and tools, making complex processes simpler.

This is a must-attend conference for professionals working with product safety, as Quality or Regulatory specialist, with design and development, clinical/ performance evaluations, post-market-clinical follow-up activities, process development or Quality Assurance/Regulatory Affairs.

Featuring insights from industry experts, legal perspectives, patient experiences, and Notified Bodies, our agenda covers key activities in both the pre- and post-market phase.

Seats are limited! Register now to secure your spot and stay ahead in the world of medical device innovation.

Featured speakers:

• Sharmila Gardner, Technical Documentation Manager & Head of UK Approved Body, from Intertek Medical Notified Body
• Pontus Gedda; Medical Device Specialist, from RISE Research Institutes of Sweden
• Anna Kuptel, Team Leader Site Auditor, from TÜV SÜD
• Richard Holborow, Global Head Clinical Compliance, from BSI
• Judith de Wilde, Attorney at law – Axon Lawyers
• Sandra Larsson, Consultant & Life Science Industry Lead – Technia
• Erik Hansson, Senior Expert in Global Harmonisation of Medical Device Regulations
• Azadeh Hajipour, Senior regulatory consultant – Key2Compliance
• Henrik Eriksson, Dialysis patient from Njurförbundet
• Dr Madlon Timme & Dr. Kristina Then, GBA Medical Device Services