How Ready Are You for UDI?

During a July 2011 GHX webinar on the clinical importance of FDA’s unique device identification system (UDI), the organization conducted an informal poll of the healthcare providers and suppliers in attendance to assess their readiness for UDI implementation.Among the suppliers, the poll found:

Karen Conway

February 27, 2012

1 Min Read
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  • No suppliers surveyed indicated that they were UDI ready

  • 44% were planning or preparing for UDI implementation

  • 4% had secured senior leadership support for UDI implementation

  • 35% had engaged in information UDI education

  • 17% stated that they were not getting ready for UDI

On the provider side:

  • 3% indicated they were UDI ready

  • 13% said they were planning or preparing for UDI implementation

  • 35% had secured senior leadership support for UDI implementation

  • 30% had engaged in information UDI education

  • 19% stated that they were not getting ready for UDI

When suppliers were asked what the biggest barriers were to UDI implementation:

  • 39% said competing priorities

  • 26% said lack of resources

  • 23% said lack of know how

  • 7% said lack of leadership support

  • 3% said lack of awareness

  • 3% said that UDI was not an immediate priority

The provider responses were as follows:

  • 15% said competing priorities

  • 37% said lack of resources

  • 20% said lack of know how

  • No providers said lack of leadership support

  • 13% said lack of awareness

  • 15% said that UDI was not an immediate priority

When asked what the biggest driver was for UDI implementation, the supplier responses were as follows:

  • 72% said regulatory compliance

  • 15% said supply chain

  • 17% said both regulatory compliance and supply chain

The provider responses were as follows:

  • 30% said regulatory compliance

  • 15% said supply chain

  • 2% said clinical

  • 50% said both clinical and supply chain

  • 3% said they had no drivers

Return to the main article, "ID Standards Have Moved Beyond a 'Nice to Have'"

About the Author

Karen Conway

Karen Conway is vice president of industry relations at GHX, where she works with standards bodies, government agencies, academic researchers, and trade associations. She is a recognized expert and speaker on the topic of Unique Device Identification and the benefits that can be delivered across healthcare with data on real-world performance of medical-surgical products.

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