10th Annual Medical Device Packaging Conference

May 6-7, 2020 | Chicago, IL

10th Annual Medical Device Packaging Conference
May 6-7, 2020 | Chicago, IL

Request Invite

WE GUARANTEE 100% PRIVACY, YOUR INFORMATION WILL NOT BE SHARED

“There are some viable solutions out there and it’s great to know how to tap into them and how others have done so. I gained much insight and useful information from others who attended and participated. It was a very nice event. Q1 did a great job coordinating it.”

Manager, Labeling & Packaging
Animas

“I took a lot of good and practical information out of the discussions, very useful.”

Manager, Technical Communications
Medtronic

 

“It was a fun to be part of a well-organized event and in the company of knowledgeable industry professionals, thanks again!”

International QA Compliance Manager
Instrumentation Laboratory

“The peer to peer conversations were great! I liked hearing the different feedback.”

Global Labeling Manager
Intuitive Surgical

“Great insight to other company experiences.”

Labeling Specialist
Edwards Lifesciences

About the Conference:

The complexity of medical devices has vastly increased over recent years due to the advancement of overall available technology that can be incorporated into product designs. While the evolution of innovation within the medical tech industry offers great benefit to healthcare providers and patients, the challenges associated with ensuring uninterrupted product safety and quality become more complicated. Packaging executives must take into consideration a variety of influences such as regulatory requirements, sterility and human factors when finalizing product packaging and distribution processes to ensure overall device quality.

Core Topics to be Addressed:

  • Integration of end-user considerations during human factor validation
  • Highlighting compliance with ISO 11607 and sterile barrier verification
  • Best practices in medical device package testing methodologies
  • Enhancing collaboration between labeling and packaging teams
  • Risk-based medical device packaging testing requirements

Program Highlights:

  • Varied perspectives from medical technology manufacturers
  • Co-located with Annual Medical Device Labeling conference
  • Interactive discussions to foster group sharing amongst attendees

Core Topics to be Addressed:

  • Integration of end-user considerations during human factor validation
  • Highlighting compliance with ISO 11607 and sterile barrier verification
  • Best practices in medical device package testing methodologies
  • Enhancing collaboration between labeling and packaging teams
  • Risk-based medical device packaging testing requirements

Request Invite

WE GUARANTEE 100% PRIVACY, YOUR INFORMATION WILL NOT BE SHARED

Audience

75 Attendees

All attendees come directly from medical device 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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