UDI Clock | GHX
The clock is ticking.
Are you UDI ready?
SEP 24 2016
The FDA UDI deadline for Class II medical devices is fast approaching.
Does your UDI submission strategy support future global requirements, as well as meet the immediate needs of today?

Industry Leadership Position White Paper
The immediate need is obvious – to create, transmit and track GUDID submission data – but for long term benefit, a strategy that satisfies regulatory and data sharing requirements as well as a sound process implementation is needed.
Download our white paper to learn more.
New Systems & Processes
Product Data Harvesting
Precise Data Formatting
Data Accuracy
Readiness Checklist
How does your strategy line up? Check out our Readiness Checklist with nine tips for developing a UDI submission plan that accomplishes both today's needs and tomorrow's goals
Download the list
Highlights from Developing Your UDI Strategy
Check out the following sound bites from the GHX webinar hosted by AdvaMed. Industry experts, Karen Conway and Denise Odenkirk, discuss strategies for working in a regulated and commercial world.

Experience gained from over 15 years of working with healthcare and regulatory groups has gone into the development of our UDI submission solution, and our solution offers the only GDSN-certified data pool focused solely on healthcare. We have and continue to play an active role in FDA efforts to develop and test the GUDID.

  • Utilize a single process for delivering device data for regulatory and industry needs
  • Access a rapid path to GUDID submission leveraging GHX UDI expertise and data
  • Work with the trusted name in healthcare data management – GHX
Contact GHX today

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