Join Us at the 2020 UDI Conference co-Located with the MDR & IVDR EU Conference!

Dates & Location to be Announced

The annual UDI Conference is the ONLY event dedicated to guidance and training for those impacted by the UDI Regulation!

Features of the 2019 UDI Conference will include:

Ample networking opportunities with the FDA UDI Team
Details on industry conversations and customer relationships that are defining UDI discoveries and driving UDI adoption
The influence of UDI across the healthcare eco-system; from point of manufacture, to point of consumption, and downstream to the clinical registries
Global UDI-related standards development and how your organization can harness harmonization efforts
Specific implementation guidance for the EU MDR & IVDR Regulations
Stakeholder activities concentrated on the quality, usefulness, accuracy, and management of the data within the GUDID
Public-private collaboration and pilot programs underway, such as AHRMM’s Learning UDI Community (LUC), that will share best practices, infrastructure improvements, new processes & growth opportunities, and activities driving UDI implementation expansion.

Learn how device manufacturers, distributors, and hospitals will be able to facilitate the following with a UDI system:

The UDI Conference attracts medical device manufacturers, distributors, GPO’s, and hospital systems that are impacted by the regulation.

Medical Device Manufacturers facing the UDI requirement should attend to understand the UDI rule and how to implement from the point of manufacturing and out to the customers.
Health Care Distribution/Group Purchasing Organizations should attend to understand and implement the UDI rule as a reseller and repackaging of medical devices.
Hospitals and Health Care Providing Organizations should attend to learn about putting UDI to work in the hospital setting for improved patient safety and operating efficiency.
Health Care Industry Professionals should attend to understand and implement UDI within their disciplines.