Additive / 3D Printing Manufacturing and Its Regulatory Issues 2019

  • 05 Mar 2019
  • Webinar

Description

Additive / 3D Printing Manufacturing and Its Regulatory Issues 2019 is a webinar that covers topics such as:

  • The Design-to-Device Process
  • What is Additive Manufacturing / 3D Printing
  • Printing Characteristics and Parameters
  • Methodologies and Materials; Recycling
  • Standard vs. Patient-Matched Devices
  • Unique Device Build Characteristics
  • Physical and Mechanical Assessment of the Finished Device
  • Unique Software Considerations
  • Validation / Revalidation
  • Acceptance Activities; Test Coupons
  • Submission Requirements

Additive / 3D Printing Manufacturing and Its Regulatory Issues 2019 intended for:

  • Quality Departments
  • Research and Development Departments
  • Manufacturing Departments
  • Regulatory Affairs Departments
  • Engineering Departments
  • Production Departments
  • Purchasing Departments
  • Operations Departments
  • Medical products consultants (primarily devices)

Past Events

Important

Please, check "Additive / 3D Printing Manufacturing and Its Regulatory Issues" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Innovations, Operations, Quality assurance
Health & Medicine: Medical technology
Science: Engineering

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