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Regulating 3D printed medical devices: an interview with Graeme Tunbridge (MHRA, UK)

In this interview with Graeme Tunbridge (Medicines and Healthcare products Regulatory Agency; London, UK), Graeme discusses the differences between standard medical devices and 3D printed devices as well as regulatory challenges, liabilities and responsibilities before postulating on the future regulatory landscape of 3D printed medical devices.

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Jan 15, 2019
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