How to Submit Data to the Global Unique Device Identification Database

The FDA UDI compliance deadline for some medical devices is a few short months away. According to the UDI Final Rule, data for medical devices must be submitted to the Global Unique Device Identification Database (GUDID). This webinar will address everything you need to know to submit data to the GUDID.

The discussion will include:

• Overview of FDA’s GUDID
• Account and device identification record modules
• How to collect, analyze, validate and submit data
• Q & A session

About the Presenter:

The featured speaker, Jay Crowley is the Vice President of UDI Solutions and Services at USDM Life Sciences. Jay was Senior Advisor for Patient Safety in the Food and Drug Administration’s Center for Devices and Radiological Health. Jay developed the framework and authored key requirements for the FDA’s Unique Device Identification system.

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    I have had the great pleasure to work with Bob for 5 years in his position of VP of Quality at Fisher Packaging Services while I acted as Director of Quality services at a sister…
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