FDA Regulation, 3D Printing and Medical Devices

7 years ago Posted By : User Ref No: WURUR12192 0
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  • TypeWebinar
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  • Location New York, United States
  • Price
  • Date 07-06-2017
FDA Regulation, 3D Printing and Medical Devices, New York, United States
Webinar Title
FDA Regulation, 3D Printing and Medical Devices
Event Type
Webinar
Webinar Date
07-06-2017
Last Date for Applying
07-06-2017
Location
New York, United States
Organization Name / Organize By
Compliance Global Inc.
Organizing/Related Departments
Compliance Global Inc.
Organization Type
OTHERS
WebinarCategory
Both (Technical & Non Technical)
WebinarLevel
All (State/Province/Region, National & International)
Related Industries

Medical/Healthcare/Hospital

Location
New York, United States

Overview

This webinar on 3D printing will cover FDA's expectations regarding the design, manufacture, testing and approval of 3D printing medical devices.

Why Should You Attend

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?

Areas Covered in this Webinar

An Introduction to 3D Printing (includes brief history, applications, types of 3D printers, 3D printing process, terminology, advantages and challenges)

An Introduction to Medical Devices & Overview of Medical Device Regulation in USA (what are medical devices, medical device classes and types of medical device submissions to US FDA)

3D Printing of Medical Devices & FDA’s current thoughts (including technical design, manufacture and testing considerations for approval)

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

For more detail please click on this below link: http://bit.ly/2pWRCE3

Email: [email protected]

Toll Free: +1-844-746-4244

Tel: +1-516-900-5515

Fax: +1-516-900-5510

Others Details

This webinar will cover FDA's expectations regarding the design, manufacture, testing and approval of 3D printing medical devices. Call +1-844-746-4244

Registration Fees
Available
Registration Fees Details
Live Session for one participant Price: $199 Corporate Live Session Group - Max 10 Participants from one Location.(For multiple location please contact our customer support team) Price: $549 Recorded Session Get unlimited access to the link for six months. Login information will be shared 24 hours after the completion of Live webinar. Price: $219 Training CD Free shipment within 72 Hours, from the date of webinar completion Price: $399
Registration Ways
Email
Phone
Website
Post Box
Other
Address/Venue
  Online Webinar 
Official Email ID
Contact
Compliance Global Inc.

2754 80th Avenue, New Hyde Park, NY 11040

[email protected]

   5169005515      5169005515
   Fax No: 5169005515
Compliance Global Inc.

2754 80th Avenue, New Hyde Park, NY 11040

[email protected]

   5169005515      5169005515
   Fax No: New York