February 27, 2018

Webinar | Device Labeling And The MDR: Your Questions Answered

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When: Wednesday, Feb. 28, 2018

Time: 9:00 am – 9:45 a.m. CST

Register Here

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:

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.

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