Learn From Our UDI Experts!
UNIQUE DEVICE IDENTIFICATION (UDI)
Best Practices for Preparedness, Project Management,
and Regulatory Compliance
New Date! Tuesday, October 15, 2013 – 8:30 a.m. to 12 p.m.
Morristown Hyatt at Headquarters Plaza
3 Speedwell Avenue, Morristown, New Jersey
This informative three-hour seminar will provide clear insight into the newly passed FDA rule for Unique Device Identification and address best practices that medical device companies can put in place to comply with this industry-changing regulation. The $99-per-attendee registration fee includes breakfast and lunch.
Tom Beatty: UDI Subject Matter Expert
Tom Beatty serves as Sr. Principal, UDI Compliance at QDevice, a division of QPharma. A subject matter expert on all aspects of UDI compliance and standards, Tom previously oversaw a successful labeling process redesign project at Novartis Pharmaceuticals. He also served as a Principal, Life Sciences Practice at Business & Decision.
Bruce Fieggen: Project Management Thought Leader
Bruce Fieggen serves as Vice President, Project Management at QPharma, and has been with the company for more than 10 years. A seasoned project management trainer and thought leader, he has planned and executed medical device projects for some of the world’s top device and life sciences manufacturers.