Medical Device Regulation's Potential Impact on Additive Manufacturing
11 June 2018 06:09:56 EDT
When the European Union's (EU's) Medical Device Regulation (MDR) was first introduced in 2017, it set in motion a three-year countdown to its full application in 2020. The MDR could drastically impact the way medical devices are made in the EU, particularly those produced using additive manufacturing (AM).
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