If you have previously registered for this event, please login below:

If you have NOT previously registered, please fill in the questions below and hit the "Register" button.

First Name*
Last Name*
Postal Code*
Work Phone*
What is the worldwide revenue of your company
What best describes your department
What kind of tool or technologies do you use for regulatory submission
I understand that by registering for this web site, I am submitting the information above to UBM Canon and to Dassault Systemes, as sponsor of the webinar. Each company may contact me, including by email, about products and services that it thinks may be of interest to me.
Please enable Cookies in your browser before registering for the webcast.
*Denotes required.

UBM Canon Privacy Policy
Dassault Systemes Privacy Policy

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

Jay Crowley
Vice President and UDI Practice Leader
USDM Life Sciences

Cathi Crist
Partner and Medical Device Industry Lead

Julie Fraser

IYNO Advisors