Best Practice 2 - Best Practice Guidance for UDI Compliance – published in Med-Tech Innovation

Best Practice Guidance for UDI Compliance – published in Med-Tech Innovation

The system means that by 2020 most medical devices will need to include a Unique Device Identifier (UDI) in human and machine-readable form. In addition, device labellers must submit mandatory data about each device to the FDA/National Library of Medicine’s Global Unique Device Identification Database (GUDID), enabling the public and healthcare stakeholders to access and download device information.

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This article was published on October 3rd, 2017