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UDI Implementation

Zoom in  Zoom out Publish date: 2014-12-17   Hits: 9   Status: Status
Date 2014-12-17 to 2014-12-17
City Palo Alto
Address 2600 E. Bayshore Road,Palo Alto, CA 94303
Exhibition hall 2600 E. Bayshore Road,Palo Alto, CA 94303
Sponsor ComplianceOnline

Event Description
This webinar on UDI implementation will discuss the new requirements set by FDA for Unique Device Identification. Attendees will learn to overcome hurdles in implementing the new process and learn best practices too.

Why Should You Attend:

The US FDA issued the final regulations for Unique Device Identification (UDI). Now is the time for manufacturers to start implementation planning.

UDI implementation for a company will have three major elements:

  • Putting the required information on the device label, the device packaging, and, in some cases, on the device itself
  • Loading all the required information into the FDA-CDRH database called GUDID
  • Revising all the affected procedures

Who Will Benefit:

This webinar will benefit the professionals working in medical device industries.

  • Regulatory managers
  • Design engineers
  • Labeling specialists
  • Project managers
  • Quality managers
Daniel O' Leary is president of Ombu Enterprises, LLC, a company offering training and execution in operational excellence, focused on analytic skills and a systems approach to operations management.

Use coupon code 232082 and get 10% off on registration.

Contact information
Contact: Referral
Address: 2600 E. Bayshore Road,Palo Alto, CA 94303
Tel: +1-888-717-2436
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