Webinar | Device Labeling And The MDR: Your Questions Answered
When: Wednesday, Feb. 28, 2018
Time: 9:00 am – 9:45 a.m. CST
The EU’s new medical device regulation (MDR) represents one of the biggest regulation changes the medical device industry has ever seen. It has taken years to finalize and will take even more time to fully implement. And affected organizations have to work towards compliance largely on their own.
In this webinar, hosted by ULG’s Susan Stugelmeyer, we’re answering your MDR questions as they relate to labeling. Susan will explore the most recent updates to the regulation, strategies to best prepare for compliance, and how the MDR stands to benefit every sector of the industry.
What To Expect From This Webinar
Attendees will leave this webinar with the following:
- Answers to the industry’s most frequently asked questions about e-labeling, Unique Device Identification (UDI) and content management
- An understanding of the MDR’s updates, requirements for economic operators, and an overview of key terms
- Strategies for complying with the biggest process changes
- Confidence that they’re better prepared for any upcoming changes, and renewed inspiration to make these necessary and vital updates
Who Should Attend?
Anyone involved in the medical device industry is encouraged to attend this webinar, especially those who work in the manufacture, distribution or import of these devices.
About The Presenter: Susan Stugelmeyer
Susan Stugelmeyer has over ten years experience supporting medical device clients with account management, helping them meet their global translation initiatives. Her key areas of focus within the translation industry include driving client corporate goals throughout their global enterprise, recognizing areas of improvement and presenting solutions, and quality process.