Tim Torbenson addresses the FDA’s recent activities involving CAD/CAM laboratories and what the FDA is expecting from these labs to become compliant with regulations. He covers the new regulations and why they’ve been incorporated; which labs are exempt from these regulations; and internal manufacturing processes that put a CAD/CAM lab under FDA oversight. He also discusses what is considered a Class II medical device as it relates to the CAD/CAM laboratory; which labs are now required to implement a Quality Management System (QMS); and what qualifies as a QMS.

The fee covers one or both NADL seminars at LAB DAY West.