Company Info






  Home > Archived Webinars > Medical Device >

Packaging Considerations When Implementing UDI Requirements



 
Our Price: $395.00

Product Code: WB-7173
Qty:

Product Info
 
About the Product
Includes 1 hour and 5 minute Windows Media Video File and PowerPoint presentations for immediate download.


With phase one of the UDI program in place, medical device companies are either already implementing UDI requirements for class III devices and/or preparing for the next round of implantable, life-supporting and life-sustaining devices labeling and packaging requirements. How this new requirement is affecting packaging professionals as well as how the FDA is dealing with noncompliance is of high concern within the industry. This session will focus on the challenges specifically facing packaging professionals in regards to UDI implementation as well as examine how the FDA is handling noncompliance.
  • Lessons learned in deploying UDI requirements within a device company
  • Overcoming hurdles in materials and design to ensure UDI compliance
  • Recent interactions with FDA when noncompliance is identified

Speaker:
Dawn Fowler
Senior Manager of Labeling, Documentation, and Training
Endologix


Participants that will find this webinar most beneficial will be those involved in medical device companies. Job titles of attendees that will be most applicable for this session will be:
  • Packaging Engineers
  • Labeling
  • Regulatory Affairs



Share your knowledge of this product. Be the first to write a review »