Don’t miss your chance to attend Key2Compliance international conference, tailored to help you navigate the intricate world of medical device regulations and standards. Gain valuable insights from industry leaders who will break down complex regulatory frameworks and share the tools you need to succeed.
WHY ATTEND?
If you’re involved in Quality or Regulatory Affairs, product design, clinical evaluation, post-market follow-up, or process improvement, this conference is a must for staying ahead in your field.
WHAT’S ON THE AGENDA:
We’ve carefully curated sessions that cover key pre- and post-market activities, including:
FEATURED PRESENTATIONS INCLUDE:
– Crossing the Atlantic: European Expertise for U.S. Regulatory Success – Joel Ironstone, Avania
– Integrating AI-Based Products into Your QMS: ISO 42001 and ISO 13485 Cyrille Michaud, MD101 Consulting
– Post-Market Surveillance: What Notified Bodies Are Looking For – Richard Holborow, BSI
– MDR Technical Documentation: Success Factors and Common Pitfalls – Sharmila Gardner, Intertek Medical Notified Body
– Global Harmonization of Medical Device Regulations: IMDRF Initiatives – Erik Hansson, Senior Expert
– Product Liability in the Medical Device Supply Chain: Navigating Change – Judith de Wilde, Axon Lawyers
SEATS ARE FILLING UP – DON’T MISS YOUR OPPORTUNITY!
The conference is fast approaching ⏳, and seats are limited. Act now to secure your spot and be a part of this key event in the medical device industry.