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
Speaker
  • 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.

About The Host
  • DGSHAPE, A Roland Company

    DGSHAPE Americas is the sales, marketing and service division for Roland DGA’s DGSHAPE dental products. DGSHAPE dental mills and accessories are the leading choice of dental labs worldwide.

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