Navigating Innovation: Deep dive into Opportunities and Challenges within the Regulatory Landscape

Navigating Innovation: Deep dive into Opportunities and Challenges within the Regulatory Landscape

In a rapidly evolving landscape, the medical device industry is at the forefront of innovation, regulation, and transformative change.

Join us for a comprehensive webinar with Qserve Group that delves into key aspects shaping the future of medical devices. Our program unfolds across four crucial topics, promising insights, expertise, and a deep dive into the regulatory intricacies surrounding this dynamic field.

Our webinar will tackle these points, focusing on:

Part 1: Innovative Medical Devices

• Overview of current trends in medical device innovation
• Case studies 
• Triggers for innovation and how to navigate 
• Opportunities and regulatory challenges in bringing innovative devices to market

Part 2: Testing for Device Safety & Compliance

• Importance of rigorous testing in ensuring device safety and compliance
• Overview of TÜV SÜD’s comprehensive testing capabilities
• Importance of pre and post-market clinical studies

Part 3: MDR Transitional Period

• What do customers need to take note of
• Notified Bodies capacity: How can companies rely on TÜV SÜD to bring products to market?

Part 4: Annex XVI

• Understanding annex XVI and its significance
• Regulatory implications and compliance strategies