Working Within FDA Regulations in the CAD/CAM World
Note: This seminar is from a past LAB DAY show
CAD/CAM technology has become so easy to incorporate into laboratories that some owners put the cart before the horse and buy equipment before understanding the regulations that may go with it. From printing models to customizing implant abutments, Gary Morgan, CDT, CQA/ASQ, covers the FDA requirements and implications for CAD/CAM in the laboratory, how to incorporate it into manufacturing processes, and understanding your machines in relation to FDA regulations.
- Approved for 1 Regulatory Standards credit
Gary Morgan
Vice President & Senior Consultant at SafeLink Consulting, Inc. · Cumming, GA
Gary Morgan, CDT, CQA/ASQ, is the Co-Owner of SafeLink Consulting, Inc. He is an Authorized Trainer under OSHA’s Outreach Program, a certified DAMAS consultant and auditor, and a Certified Quality Auditor.