By Adam J. Penna

Quality and regulatory are critical to the use of additive manufacturing application for medical applications. Adam Penna gets a preview from Laura Gilmour on two critical discussions at the AM Medical Summit: Where Medicine & Technology Meet to Transform Lives November 1–3, 2022

0:21 – Panel 1 preview:

QMS Approaches for Point-of Care 3D Printing

Wednesday, November 2, 2022 1:30 PM to 2:15 PM · 45 min. (US/Central)

Every hospital has a critical quality program for patient care. What does this mean for 3D printing at the point of care? What are the approaches, processes, and tools you can use to assure your 3D printing meets the expectations of every healthcare professional?

MODERATOR: Laura Gilmour, Medical Additive Manufacturing & Regulatory Strategies Consultant, LG Strategies

PANELISTS: Daniel Rosen, MD, Associate Professor, Baylor College of Medicine; Gregory Voss, Research Engineer, MADE Program, Minneapolis VA Health Care System, Minneapolis VA Health Care System; Ben Johnson, Vice President of Portfolio & Regulatory, 3D Systems

4:00 – Panel 2 preview:

How Does Regulatory Compliance Impact Your 3D Printing?

Wednesday, November 2, 2022 11:00 AM to 11:45 AM · 45 min. (US/Central)

As 3D printing medical and dental applications grow, understanding regulatory compliance is critical. What’s the difference between custom and patient-specific devices? Do both need clearance? Are there are their differences between countries? Do the same requirements apply at a manufacturer, dental lab, and hospital?

MODERATOR: Kim Torluemke, Medical Devise Regulatory Professional, KT Regulatory Consulting

PANELISTS: Joel Anderson, Biomedical Engineer/Premarket Reviewer, US Food and Drug Administration; Laura Gilmour, Medical Additive Manufacturing & Regulatory Strategies Consultant, LG Strategies

More Details: https://events.additivemanufacturing.com/medical/