EUDAMED 2024 and Beyond Preparing for the Future of Medical Device Oversight

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Course Overview

Are you ready to enhance your knowledge of the European Database for Medical Devices (EUDAMED) and how it can revolutionize device compliance in the EU market?

Dive deep into the core of EUDAMED during this webinar as we dissect its modular architecture, including key modules such as Actors, UDI/Device Registration, Notified Bodies and Certificates, Clinical Investigations and Performance Studies, Vigilance and Post-Market Surveillance, and Market Surveillance. Discover how these modules reshape regulatory processes and strengthen device oversight across the EU.

Uncover the latest updates on EUDAMED’s implementation timeline and how they may impact your compliance strategy. Explore the pivotal role of the Unique Device Identification (UDI) system in driving traceability, enhancing patient safety, and improving healthcare outcomes under the Medical Device Regulation (MDR) and the In Vitro Diagnostic Regulation (IVDR).

Join us for this comprehensive session that offers insights into the current landscape and future projections of EUDAMED. In this exclusive webinar in partnership with Honeywell | Life Sciences, you will gain practical guidance on navigating compliance challenges and leveraging the system for enhanced market surveillance and optimized product lifecycle management.

Don’t miss this opportunity to stay ahead in the evolving world of medical device regulation. Register now to secure your spot at the forefront of industry innovation!

  • Medical device manufacturers and distributors
  • Regulatory affairs professionals in the medical device industry
  • Quality assurance and compliance personnel in the medical device sector
  • Healthcare professionals involved in the selection and use of medical devices
  • Industry consultants and advisors specializing in medical device regulations and quality control

Course Content

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