GS1 Standards for U.S. FDA UDI Workshop


Co-Located at the UDI Conference 2019 

This 5-hour workshop introduces you to the GS1 System and focuses on the GS1 Standards used within the context of the U.S. FDA Unique Device Identification (UDI) Rule.*

Date: June 10, 2019
Time: Noon - 5:00 PM ET
Location: Co-located with the
UDI Conference 2019 in Baltimore, MD
Cost: $295 per person

Gain a broader understanding of how GS1 Standards align with many U.S. FDA UDI Rule components 


Attendees will be introduced to the basics of the U.S. FDA UDI Rule and to those GS1 Standards that can be used to address certain aspects of the requirements for product identification, product labeling, and submission of information to the Global Unique Device Identification Database (GUDID). The workshop will also discuss the importance of data quality and data governance as components of a UDI implementation. 

Get Product Date Rigth the First Time
Understand the role that data management and quality play in a successful UDI program.
Discover how GS1 Standards align with many U.S. FDA UDI Rule components.
Learn standards for label quality and format through hands-on exercises.
Receive a bound set of workshop presentation materials, for easy reference later on.
Hear how to avoid some of the most common GUDID data issues.
Share experiences and challenges with their peers.

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Get Product Date Rigth the First Time
GS1 Connect

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  • Quis imponere tibi noverca vel pede te aetatis culpa’a commodum sint modestia/aegrotus visccra enim

Gain a Broader Understanding of how GS1 Standards Align with Many U.S. FDA UDI Rule Components 


Attendees will be introduced to the basics of the U.S. FDA UDI Rule and to those GS1 Standards that can be used to address certain aspects of the requirements for product identification, product labeling, and submission of information to the Global Unique Device Identification Database (GUDID). The workshop will also discuss the importance of data quality and data governance as components of a UDI implementation. 


Attendees can expect to:

  • Enjoy an open and interactive training environment that includes classroom-style instruction and the opportunity to share experiences with your peers. 

  • Receive a brief update on how to avoid some of the most common GUDID data issues, learn about GUDID attributes, and gain insights for your implementation.

  • Understand GS1 standards for unique identification and proper identifier formats.

  • Receive a bound set of workshop presentation materials, for easy reference when you return to your organization.

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Presenter

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Presenters

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Presenter's Really-Long Name

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Presenter's Really-Long Name

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Presenter's Really-Long Name

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Presenter's Really-Long Name

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Presenter's Really-Long Name

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Presenter's Really-Long Name

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Reserve your spot - fill out the form below.

If you can’t attend in person, register anyway and we will send you a link to the on-demand recording.

*For information about the rule, see the U.S. FDA Unique Device Identification System

Disclaimer: GS1 US is the local GS1 Member Organization that supports implementation of the GS1 System in the United States. GS1 US employees are not representatives or agents of the U.S. FDA, and the content herein has not been reviewed, approved, or authorized by the U.S. FDA.

GS1 is a U.S. FDA-Accredited Issuing Agency for UDI, and GS1 Standards are authorized for use in implementing the requirements of the U.S. FDA UDI Rule.

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