UDI Implementation

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

Who Will Benefit:

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

Regulatory managers

Design engineers

Labeling specialists

Project managers

Instructor Profile:

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. Mr O’Leary has more than 30 years’ experience in quality, operations, and program management in regulated industries including aviation, defense, medical devices, and clinical labs.

Note:

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

For Registration:

http://www.complianceonline.com/udi-implementation-webinar-training-703588-prdw?channel=sciencedz