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UDI Conference 2013
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UDI Conference 2013

The FDA UDI Regulation will establish a single device identification system that is consistent, unambiguous, standardized, and globally harmonized. All manufacturers of medical devices will be required to comply with the new UDI methodology. Participate in conference sessions led by the FDA, and pioneers in the medical device industry who will explain how UDI will advance patient safety by improving the ability to monitor adverse events and maximize the value of electronic health records.

9/19/2013 to 9/20/2013
When: 9/19/2013
Where: Hilton Baltimore
Baltimore, Maryland 
United States

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UDI Conference 2013
Baltimore, Maryland | September 19-20


The FDA UDI Regulation will establish a single device identification system that is consistent, unambiguous, standardized, and globally harmonized. All manufacturers of medical devices will be required
to comply with the new UDI methodology.

Attend the Conference to:

  • Receive an update from the FDA on current status of the Regulation
  • Grasp the fundamentals of an automated identification system
  • Understand the why's, how's & the "what's in it for me"
  • Create your plan for implementation
  • Learn how to utilize the UDI Database for success and compliance
  • Learn how to guide your organization through the UDI Regulation

Who should attend:

  • Medical device manufacturers Health care distributors
  • Group purchasing organizations
  • Hospitals and health care providers
  • Health care industry professionals


Participate in conference sessions led by the FDA, and pioneers in the medical device industry who will explain how UDI will advance patient safety by improving the ability to monitor adverse events and maximize the value of electronic health records.

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

  • Reduction of Medical Errors
  • Supply Chain management
  • Utilization of UPN and PDU data
  • Recall of Medical Devices
  • Improved Medical Device Reports (MDRs)
  • Preventing Allergic Reactions to Devices
  • Identification/Reduction of Product Counterfeiting
  • More Efficient Purchasing
  • Improved Inventory Control
  • Enhanced Medical Device Asset Utilization
  • Efficient Reimbursement
  • Identification of Compatibility Issues
  • Enhancements in Post-Market Surveillance


You can also explore the technology behind UDI in the exhibits area where you canlearn about
the solutions for your UDI implementation.


For complete conference details, visit UDI Conference 2013 today.

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