Conference: Medical Device Product Life Cycle

Join us in boosting MedTech knowledge together!

On October 8 and 9th, 2024, Key2Compliance is delighted to once again host the highly appreciated Conference, “Medical Device Product Life Cycle”, this time in Stockholm!

We’re honored to have four Notified Bodies joining us as featured speakers at our event: BSI, RISE, Intertek, and TÜV SÜD.

Featuring international representatives from the industry, a legal expert, a patient, and multiple Notified Bodies, our agenda covers key activities in both the pre- and post-market phase. Speakers include experts such as:

• Sharmila Gardner, Technical Documentation Manager & Head of UK Approved Body, from Intertek Medical Notified Body
• Richard Holborow, Head of Clinical Compliance at Global Regulatory Compliance Team from BSI
• Judith De Wilde, Attorney at law, from Axon Lawyers
• Pontus Gedda, Medical Device Specialist, RISE Medical Notified Body AB
• Anna Kuptel, Team Leader Site Auditor, TÜV SÜD
• Sandra Larsson, Business Consultant & Life Science Industry Lead, TECHNIA

Explore topics such as:  “Your MDR Technical Documentation: three success factors, and the mistake you should avoid!”, ” Outsourcing and Supplier Control – what the MDR requires, and “Product liability throughout the medical device supply chain: a changing landscape”.

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

Don’t miss out on this invaluable opportunity to enhance your expertise and network with industry leaders. Register now to secure your place!