Additive Manufacturing
& FDA Regulation of
3D Printed Medical Devices

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Event 1: State-of-the-Art Additive Manufacturing Fundamentals

10:30 – Noon
Discussion on:

• Processes and Process Capabilities
• Materials
• Biocompatibility
• Applications
• Costs/Economics
• Limitations

 

Noon – 1 p.m. Networking Lunch

Cost: $25 includes morning session registration, materials & lunch

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Event 2: FDA Perspective on Regulation of 3D Printed Medical Devices

1–2:30 p.m.
Dr. Steven K. Pollack
Director, FDA Office of Science and Engineering Laboratories

Discussion to include:

• Additive Manufacturing Advancements
• Regulatory Implications
• Materials Issues
• Patient Match vs Custom Design
• Design Fundamentals

2:45 – 4 p.m. Panel discussion featuring industry & medical device experts

No registration fees required

 

 

Presented by Austen BioInnovation Institute as part
of its ongoing Safe Harbor Seminar Series,
in association with America Makes and
Youngstown Business Incubator

Register Now!