By AuntMinnie.com staff writers

January 11, 2018 -- The U.S. Food and Drug Administration (FDA) held a webinar on January 10 reviewing its final guidance for creating medical products using 3D printers.

The meeting covered the agency's current stance on device design and manufacturing, testing considerations, and additional labeling considerations. It highlighted three significant changes to the initial guidance:

  • A new section on cybersecurity and personally identifiable information
  • Updated labeling considerations
  • The replacement of the term "cleaning" with "removing manufacturing material"

The transcript and slides from the webinar are available online.


Copyright © 2018 AuntMinnie.com
 

To read this and get access to all of the exclusive content on AuntMinnie.com create a free account or sign-in now.

Member Sign In:
MemberID or Email Address:  
Do you have a AuntMinnie.com password?
No, I want a free membership.
Yes, I have a password:  
Forgot your password?
Sign in using your social networking account:
Sign in using your social networking
account: