With the recent publishing of the European Medical Device Regulations (MDR), manufacturers have additional UDI compliance challenges. Factor in stringent demands from Russia and the Eurasian Economic Union (EAEU) and labelling gets even more complex. How much can you leverage the work you’ve already done to sustain compliance? What else is in store in the world of UDI?

Get the answers to these and other questions in this timely, insightful webinar featuring USDM Life Sciences’ Jay Crowley.

Topics will include:

  • A quick overview of MDR and EAEU requirements including upcoming deadlines
  • Comparison of US and international UDI requirements—and which require special attention
  • Implementation challenges and how some companies are overcoming them
  • Labeling strategies and technologies to meet and sustain global UDI compliance


Jay-Crowley.pngJay Crowley, Vice President of UDI Services and Solutions, USDM Life Sciences
Jay Crowley is the Vice President of UDI Services and Solutions 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.