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When: Thursday, September 29, 2016

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As medical device and diagnostic manufacturers continue to develop life enhancing products for patients across the globe, medical product
labels hold an increasingly important position in providing critical information to healthcare professionals and patients, focusing on the safe
handling and use of the device. Labeling executives strive to continuously optimize operations, to ensure a streamlined approach to label data
collection, real estate formatting as well as regulatory reviews, and face numerous challenges in achieving each step compliantly. Furthermore,
with the FDA UDI rule in place for over 2 years and ongoing implementation within medical technology organizations, lessons can be learned by
examining peers’ experiences with UDI and provide insight into solutions to maximize the corporate device identification strategy. Finally, riskbased
approaches to error minimization in label development and production is at the forefront of labeling teams’ goals, which involves many
areas to supervise such as human factor testing to ensure labels and instructions for use are compliant and intelligible to the end-user.


To provide participants with the best learning experience possible, the program will include a UDI-specific track, open to those in need of further
clarification into device identification challenges. As in all Q1 conferences, speakers from the industry, standard organizations and regulatory
bodies will provide timely insight on topics impacting labeling operations through engaging presentations and interactive sessions. Further areas
of labeling challenges will be examined in great depth and debated during lively Q&A sessions following each presentation, allowing for a
maximized number of key messages delivered on site. With labeling executives actively looking for new technology and solutions for streamlining
labeling programs, sponsors will find this conference to be an excellent business development opportunity.

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