FDA Regulation, 3D Printing and Medical Devices
WebcastFaculty
OVERVIEW
FDA Regulation, 3D Printing and Medical Devices is organized by Compliance Global Inc. and would be held on Jun 07, 2017.
This webinar on 3D printing will cover FDA's expectations regarding the design, manufacture, testing and approval of 3D printing medical devices.
The Food and Drug Administration (FDA) is responsible for the approval of medical devices in the United States of America. Today 3D printing is used in a wide variety of applications, even for the manufacture of medical devices. So what are FDA’s current thoughts regarding the approval of 3D printed medical devices?
Learning Objectives:
In this medical device compliance training, medical device manufacturers, software developers, engineers, validation experts, 3D printing raw material manufacturers and suppliers, regulatory and quality professionals, will be informed of FDA’s expectations regarding the design, manufacture and testing of 3D printed medical devices. Those interested in 3D printing technology will be well briefed too.
Who Will Benefit:
The following professionals from the Medical Device industry will benefit from this training:
• Manufacturing
• Production
• Product management
• R&D
• Software developers and vendors
• Engineers
• Validation experts
• 3D printing raw material manufacturers and suppliers
• Regulatory and quality professionals
• Anyone interested in 3D printing technology and / or medical devices
This webinar on 3D printing will cover FDA's expectations regarding the design, manufacture, testing and approval of 3D printing medical devices.
The Food and Drug Administration (FDA) is responsible for the approval of medical devices in the United States of America. Today 3D printing is used in a wide variety of applications, even for the manufacture of medical devices. So what are FDA’s current thoughts regarding the approval of 3D printed medical devices?
Learning Objectives:
In this medical device compliance training, medical device manufacturers, software developers, engineers, validation experts, 3D printing raw material manufacturers and suppliers, regulatory and quality professionals, will be informed of FDA’s expectations regarding the design, manufacture and testing of 3D printed medical devices. Those interested in 3D printing technology will be well briefed too.
Who Will Benefit:
The following professionals from the Medical Device industry will benefit from this training:
• Manufacturing
• Production
• Product management
• R&D
• Software developers and vendors
• Engineers
• Validation experts
• 3D printing raw material manufacturers and suppliers
• Regulatory and quality professionals
• Anyone interested in 3D printing technology and / or medical devices
SPECIALITIES
Healthcare Technology
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