This webinar was held on Tuesday, July 19, 2016.
Watch the on demand webinar
The FDA recently issued guidance on using 3D printing for medical applications. This webinar will give you the information and resources you need to ensure you are in compliance with these guidelines.
You will learn:
- What the FDA guidance covers as it relates to 3D printing.
- How FDA validation differs for 3D printed medical devices versus other methods of device manufacture
- The essential steps needed to validate 3D printing medical devices
Kim Torluemke, VP Quality & Regulatory, 3D Systems Corporation
Currently VP of Quality & Regulatory, Healthcare, Kim Torluemke began her career in 3D printing by leading the development effort on Medical Modeling’s first FDA cleared manufacturing project in 2008. Since, she has continued on a path of increasing quality and regulatory oversight and followed the company through a transition to join 3D Systems in April of 2014. With nearly a decade of experience in the 3D printing industry covering multiple disciplines, Kim continues to revolutionize healthcare by combining proprietary and powerful workflows to produce medical devices encompassing templates, guides, instruments, implants, and software technologies through the evolving landscape of regulation to ensure safe and effective products are available to change people’s lives. Kim received her undergraduate degree in engineering with a mechanical specialty from the Colorado School of Mines. She works out of 3D Systems’ Denver, CO Healthcare Technology Center.
Leslie Langnau, Managing Editor, Design World
Leslie has more than 20 years experience as a technical editor and trade journalist. She has reported, investigated, and written extensively on the following subjects: mechanical automation, industrial networking, additive manufacturing, and automation controls. She has a B.S. degree in Mechanical Engineering from Michigan State University.
Filed Under: WEBINARS