As the number of medical devices manufactured using additive manufacturing/3D printing technologies continues to increase, manufacturers struggle with the quality, validation, and filing processes to have each device cleared for use. This workshop brings together technology and process experts to walk participants through the considerations at every step as its applied to 3D printed devices. Discussion will include certification, validation, testing, PMA, IQ, OQ, PQ and more.
- Gain insight into FDA’s view of 3D printing as applied to medical devices
- Obtain an overview of the types of 3D printed medical devices that have been cleared
- Understand how quality, controls, validation and verification can be accomplished with 3D printing
- Learn the latest available information on regulatory clearance processes specific to 3D printing
Workshop Leader: Danielle Lucia, Materialise USA
Instructors: Matthew Di Prima, PhD, Food & Drug Administration; Scott Brewer, 3D Systems; Laura Gilmour, EOS; Dawn Lissy, Empirical