2012 UDI Conference
September 18-19, 2012
Orlando, FL
Omni Orlando Resort at Champions Gate
View the Conference Agenda here: http://udiconference.com/agenda.html
FDA's UDI proposed regulation has been published – for more information, please visit www.FDA.gov/UDI
FDA’s UDI System will transform disparate medical identification methods into a single device identification system that is consistent, unambiguous, standardized, and globally harmonized. The UDI Conference will offer you the ability for live interaction with the FDA UDI Team in advance of the close of the comment period (ends November 7th). Attend to hear from the FDA on the technical details of the Proposed UDI Regulation; how to interact with the UDI Database; the role of UDI in device identification and data quality; and open interaction for questions.
Industry leaders will share experiences of implementing UDI in the supply chain, the value of UDI in clinical information systems, and what has already been achieved. To round out the conference agenda, you will have the opportunity to hear in depth details from the leading standards organizations, including: DUNS; GMDN; GS1; HIBCC; and ICCBBA.
The UDI Regulation will require new or improved systems and processes to efficiently mark devices, scan device information at various points in its lifecycle, and transmit that data to other software systems. You will have the opportunity to understand the requirements for your automatic identification system in a session delivered by the UDI Committee of AIM North America. You can augment your understand of the enabling technologies in the UDI Conference exhibit hall.
Who should attend?
- Medical Device Manufacturers
- Healthcare Distributors
- Group Purchasing Organizations
- Hospitals and Healthcare Providers
The UDI Conference is produced and managed by The Clarion Group, Inc., (1-800-560-1980)
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