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UDI Implementation Workshop
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UDI Implementation Workshop

Bringing the UDI Regulation & the Global UDI Database (GUDID) to Life! The UDI Implementation Workshop is for Class III Medical Device Manufacturers who are in immediate need of information and guidance to meet the September 24, 2014 compliance deadline, or those that need to jumpstart their UDI adoption effort! The FDA UDI Team will be in Baltimore May 20-22 for a roll-up-your sleeves / deep-dive Workshop covering all components of the UDI Regulation and the GUDID Guidance.

5/20/2014 to 5/22/2014
When: 5/20/2014
Where: Baltimore Hilton
Baltimore, Maryland 
United States

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This Workshop is strictly focused on critical information exchange, expanded interaction, and heightened networking designed to deliver immediate and actual results in your UDI implementation initiative.


Attend the Workshop to:

  • Hear a summary of the FAQ’s processed by the UDI Help Desk to date
  • Establish a GUDID Account
  • Walk-through the Data Identifier (DI) Record
  • Discuss the GUDID HL7 SPL Submission Options
  • Learn about the FDA Data Quality Program & Specifications
  • Understand the requirements for your automatic identification systems
  • Gain insight into the Supply Chain and Healthcare Provider’s use of UDI data
  • Create your plan for UDI implementation to help guide your organization

AIM Members Receive a $100 Discount

Seating will be limited and will be assigned on a first-come, first-served basis.
Go to and enter “AIM” in the promotional code field line during online registration to receive $100 off of the rate. Register by April 30th for the best rate.


For the complete Workshop agenda and the most up-to-date information, please visit

For information on the FDA UDI Regulation, visit


The UDI Implementation Workshop and the UDI Conference are produced and managed by The Clarion Group, Inc. 1-800-560-1980.

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