Med Device Labeling Event to Feature Loftware Customer LifeNet Health

by Craig Hodgson, on May 11, 2018

Labels continue to play a critical role in the safe testing, manufacturing, distribution and use of medical devices worldwide. Not only must they comply with a range of regulatory requirements like UDI and the EU’s impending MDR/IVDR, but also meet unique customer and regional specifications. It’s an ongoing challenge for organizations—especially as they strive to improve supply chain efficiency at the same time.

That’s what events like the upcoming Q1 Productions’ Medical Device & Diagnostic Labeling Conference, May 15 – 16 in Chicago, are all about. This is the eighth consecutive year the conference has been held and, judging by the packed agenda, there is still a lot of good, relevant insight to be gained. Topics include clarifying US and EU medical device labeling requirements, targeting content towards different patient populations, and strategies for implementing the right labeling solutions.

Among the industry thought leaders, regulators and solution providers presenting, one session definitely worthTS-Q1-med-device-labeling-agenda checking out comes from LifeNet Health, a leading provider of transplant solutions. Kanchan Seshadri, Manager of Enterprise Solutions at LifeNet Health, will deliver a case study “Managing the Full Product Label Lifecycle with Confidence” during which she’ll highlight how her company has greatly improved the process of designing, managing and printing labels in a validated environment. You’ll learn how the company is able to meet changing customer and regulatory requirements—many of the same challenges you’re facing—with improved accuracy, agility and consistency.

If you are planning to attend the event, make sure you circle your agenda for Kanchan’s presentation, Wednesday, May 16th at 10:15 AM. You’ll also have the opportunity to ask questions and follow up with Loftware to see how LifeNet’s Spectrum labeling solution can be configured to meet your own requirements.

We look forward to seeing you there! If you can’t make it, we invite you to take a look at our new white paper co-developed with Jay Crowley from USDM Life Sciences “Navigating Global UDI Requirements: How Enterprise Labeling Helps Sustain Compliance and Optimize Supply Chain Performance.”  It’s a great read that will benefit your efforts to be more strategic with your extended supply chain labels.


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Topics:Medical DevicesRegulatory