NXP at MEDICA 2024

MEDICA 2024

November 11-14, 2024, Düsseldorf, Germany

  • MEDICA2023 logo

    MEDICA  is one of the largest medical B2B trade fairs in the world and brings together more than 83,000 visitors to network, discover latest innovations and deepen industry knowledge. The event is taking place at the Messe Düsseldorf from November 11-14, 2024.

Visit the NXP Booth

Come by NXP‘s Booth B22 (Hall 13) and explore NXP's cutting-edge semiconductor solutions to advance medical IoT devices and medicinal products to enable efficient processes, reliable product protection, and improved patient safety and outcome with low-power efficiency, intelligence, security and wireless connectivity.

Explore NXP On-Site Demos

Experience NXP’s Solutions For

  • Home medical monitoring and treatment to improve personal health with smart self-care and remote monitoring .
  • Hospital diagnostic, monitoring and therapy to advance patient and product safety with operational efficiency.

NXP at MEDICA Tech Forum

Get more details on our sessions at the MEDICA Tech Forum

Accelerate Digital Healthcare through Edge AI

Presented by: Pierluigi Gardella, Global Marketing & Engineering Director, System Solutions for Healthcare at NXP
Tuesday, Nov 12, 4:40-5:00 PM, Hall 9 / D10

Explore how edge AI can transform elderly care by enabling real-time health monitoring, early detection of conditions, and personalized treatment, all while maintaining data privacy. The lecture will highlight how these technologies empower caregivers with immediate insights, reduce their workload, and improve the quality of life for elderly patients through more responsive, home-based care solutions.

IoMT Security: Navigating FDA and EU MDR Cybersecurity Recommendations

Presented by: Giuseppe Guagliardo, Senior Product Manager NFC IoT Security at NXP
Wednesday, Nov 13, 4:00-4:20 PM, Hall 9 / D10

The Internet of Medical Things (IoMT) is transforming healthcare, making cybersecurity paramount for safeguarding patient data and device functionality to ensure patients’ safety. Both the U.S. Food and Drug Administration (FDA) and the European Union’s Medical Device Regulations (EU MDRs) are addressing these concerns through stringent cybersecurity recommendations and best practices. In this session, we will explore key regulatory expectations, essential cybersecurity guidelines and security best practices that medical device manufacturers must adhere to when developing secure IoMT architectures to ensure patient safety and standards compliance.