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UDI Lessons Learned: Keys to Gaining and Sustaining Compliance


Date: September 25, 2014
Time: 8:00 AM PDT | 11:00 AM EDT
Duration: 45 minutes


Sponsored by:



About this webinar

The final rule has been issued by the FDA – medical devices distributed in the US must carry a Unique Device Identifier, or UDI. But the implications of the rule go well beyond the requirement to include a unique numeric or alphanumeric code. By incorporating UDI information on medical devices, the ultimate benefit is the direct impact on the end users – the patient. How are you supporting this new regulation? And are you prepared for regulations of the future?

Key take-aways:
  • UDI impacts far more than labeling and tracking - what you need to know
  • Preparing for GUDID submission may be harder than you imagine
  • The work is not over at the UDI deadline for your class of devices – learn what’s critical next

Speakers
Jay Crowley
Vice President and UDI Practice Leader
USDM Life Sciences




Cathi Crist
Partner and Medical Device Industry Lead
Kalypso




Moderator:
Julie Fraser
Principal
IYNO Advisors