Webinar | Direct Part Marking for FDA UDI Compliance
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Webinar | Direct Part Marking for FDA UDI Compliance

 Export to Your Calendar 6/26/2018
When: 06/26/2018
12:00 pm
Where: Teleconference Webinar
United States


Online registration is available until: 6/26/2018
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Direct Part Marking for FDA UDI Compliance | A Town Hall Webinar


Tuesday June 26th | 12:00 Noon ET

 

One of the most reliable ways to ensure a UDI lasts the lifecycle of a device is by affixing a permanent mark to the device. Direct part marking (DPM) is not a new concept but is relatively new territory for many medical device manufacturers. AIM North America has assembled an expert panel who will discuss how AIDC technologies, such as DPM, into your compliance strategy will help you meet the next UDI compliance deadline.

 

This Town Hall will discuss:

  • Regulations and deadlines
  • AIDC technology options
  • Current DPM standards
  • DPM applications and best practices
  • Steps in a DPM project plan
  • Audience Q&A

Featured Speakers

Moderator | Ardi Batmanghelidj | Innovatum

 

Panelists       
Jay Crowley | USDM Life Sciences

 

Pat Cairns | Matrix IT Tracking Systems

 

Patrick Schlather | FOBA

 

Webinar Presenting Sponsor

 

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