On-Demand Webinar
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).
Don’t miss this opportunity to stay ahead in the evolving world of medical device regulation.
