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Final Rules of Unique Device Identification

  December 05, 2017  
Netzealous LLC DBA - Compliance4All, Online

This webinar will address the four key steps to compliance by device 

manufacturers. Also covered will be the Final Rule's provisions to 

address existing FG inventory, not properly labeled. 

Why should you Attend:
It will also review the implementation schedule which is required of 

medical device companies selling products in the U.S. This is a major 

change for medical device manufacturers, with far-reaching effects in 

regulatory compliance, as envisioned by the FDA.

Areas Covered in the Session:
Learn the basic requirements of UDI Labeling and its Database
UDI / GUDID Implementation Schedules
Required steps for UDI / GUDID compliance by the Medical Device 

Future Requirements

Who Will Benefit:
CGMP Responsibilities
CROs and Clinicals Personnel
Medical Personnel
Other Healthcare Professionals
Staff and Office Personnel

Event Fee: One Dial-in One Attendee Price: US$150.00

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com
Organized by: Compliance4All
Invited Speakers:
Speaker Profile:
John E. Lincoln is a medical device and regulatory affairs consultant. He 

has helped companies to implement or modify their GMP systems and 

procedures, product risk management, U.S. FDA responses. In 

addition, he has successfully designed, written and run all types of 

process, equipment and software qualifications/validations, which have 

passed FDA audit or submission scrutiny, and described in peer-

reviewed technical articles, and workshops, world wide.
Deadline for Abstracts: 2018-02-13

Full Details & Registration Link:


E-mail: support@compliance4All.com
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