该网络研讨会于2016年7月19日星期二举行。
观看随需应变的网络研讨会
FDA最近发出了使用3D打印进行医疗应用的指导。此网络研讨会将为您提供所需的信息和资源，以确保您遵守这些指南。
你将学习：
- FDA指导涵盖的内容与3D打印相关。
- FDA验证如何对3D打印的医疗设备而言，与其他设备制造方法相比
- 验证3D打印医疗设备所需的基本步骤
演讲者
Kim Torluemke副总裁质量和监管，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，总编辑，设计世界
Leslie有超过20年的技术编辑和贸易记者经验。她在以下主题上进行了广泛的报道、调查和写作:机械自动化、工业网络、增材制造和自动化控制。她拥有密歇根州立大学机械工程学士学位。
提交：网络研讨会
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