In this informative session, our presenter will provide a high-level summary of Unique Device Identification (UDI) related activities around the world, including UDI plans and timelines for various regulatory authorities and commercial trading partners.
Attendees can expect an up-to-date timeline for global UDI regulations by class, critical differences in compliance policies, datasets, maintenance requirements, and specific direction as to what this means for medical device manufacturers looking to market their products internationally. This knowledge can be applied to inform their approach to global regulations for Unique Device Identification.
Learning Objectives:
Know and plan for numerous global UDI/device registration requirements around the globe
Prepare support for diverse Health Authority UDI reporting and update policies
