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US FDA Draft Guidance Tackles Medical Device 3-D Printing

This article was originally published in Clinica

Executive Summary

The US FDA has published a draft 'leapfrog' guidance on 3-D printing of medical devices that draws from a 2014 agency workshop on the topic. The guidance outlines key issues manufacturers should think about when designing products made with 3-D printers, including the materials used to make those devices and considerations when planning devices specific to individual patients.

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