Contact Us   |   Print Page   |   Sign In   |   Join
Webinar: CDRH Industry Basics Workshop on Unique Device Identification
View Registrations Tell a Friend About This EventTell a Friend
Webinar: CDRH Industry Basics Workshop on Unique Device Identification

When: January 27th, 2016
From 1:00 PM until 3:00 PM
« Go to Upcoming Event List  

This workshop (presented by webinar) will provided information on the fundamental concepts of Unique Device Identification and how to prepare for and request a GUDID account.

The workshop features two sessions, each consisting of a presentation followed by a question and answer session with a panel of experts from the Office of Surveillance and Biometrics. Participants can email or call with questions during each session’s Question and Answer session.

Participants chose one or both of the sessions. Each session will begin at the scheduled time.

1:00 – 2:00 PM – Unique Device Identification (UDI) System Regulatory Overview
2:00 – 3:00 PM – GUDID Account Request: Preparation and Process

Target Audience: Medical Device Industry, Medical Device Industry Associations, Class II Labelers other than Implantable, Life Supporting, and Life Sustaining Devices.

There is no fee to attend and registration is not required.

How to Join the Workshop: All participants attend via webinar, CLICK HERE.                       

The January 27, 2016, CDRH Industry Basics Workshop is not intended to provide submission-specific feedback, so please limit your questions to broad policy questions about the program topics. Submission-specific questions will be referred to the appropriate CDRH program Office for response.

Creating Value
by delivering business-critical resources & bottom line savings
Building Networks
by connecting Michigan's bio-industry one member at a time
Growing Talent
by creating opportunities that develop people & build organizations
Membership Software Powered by YourMembership  ::  Legal