Forum considers global UDI framework for medtech

04/29/2013 | Clinica (subscription required)

Draft guidance on the unique device identifier system for medical devices, designed to set nonbinding policies to aid regulatory authorities in creating their own UDI programs, is under consideration by the International Medical Device Regulators Forum. Review of the UDI document, which also aims to promote a consistent UDI approach worldwide, is set to be completed July 31.

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