9th Annual Medical Device and Diagnostic Labeling Conference

May 14-15, 2019 | Chicago, IL
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“I thought the conference was excellent!  Having a conference tailored to one discipline made each panel and contact relevant.” Director, Compliance & Legal Affairs Orexigen
“Great insight to hear payer perspective in contracting and account management and the changing healthcare landscape.” Channel Liaison Biogen
“It was definitely an excellent well-rounded opportunity to meet new people, get new ideas, and get an in-depth education on what’s to come with the FDA collaborations.” Quality Engineer Centurion Medical Products
“It was very well organized event and high quality, the fact to have an IVD track was also interesting. Thanks, I will recommend the Q1 event!” Regulatory Affairs – EMEA Regional Head BIOMERIEUX
“The organization and support staff were fantastic! I’m looking forward to next year.” Global Business Project Lead Genentech

About the Conference:

With the goal of ensuring safe use of medical technology, regulatory authorities on an international level continuously release new provisions impacting label content, prompting teams to develop increasingly flexible strategies in order to reach compliance in a timely manner. Challenges therefore reside in remaining abreast of rapidly evolving rules, correct interpretation and integration of provisions in corporate strategies, all while maintaining efficiency in ongoing labeling operations. In particular, the recent shift in regulations in Europe generate much concern from labeling professionals, unsure how to move forward with a lack of clarity in specific areas of the MDR and IVDR, such as the use of symbols.

Topics to Be Addressed:

  • Deep Dive into EU MDR & IVDR Impact on Labels
  • IFU Content Optimization: Human Factors & Technical Writing
  • Tech Talks: Opportunities in Label Optimization Technology
  • Beyond EU: International Labeling Concerns in China & Russia
  • Maximizing Label Content Localization through Flexibility
  • Enhancing eLabeling Strategies for US Based Products

Program Highlights:

  • 2018 Program Included over 200 Total Participants
  • More than 900 Individuals Have Participated in the Training
  • Over 50% of Participants Have 20+ Years Industry Experience

Audience

75 Attendees

All attendees come directly from medical device and diagnostic companies

Distinguished Presenters

Speaker recruitment in process

Networking

Networking time is built into the agenda to allow industry peers to connect and exchange ideas

Open Dialogue and Group Share

Each presentation is followed by 10-15 minutes of open dialogue for questions and exchange of best practices

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