Whitepaper: UDI – from the basics to the benefits
Posted: 22 December 2021 | SoftGroup | No comments yet
Get the most detailed information about UDI – requirements, implementation and benefits. Everything that supply chain participants need to know!
With the implementation of the Medical Devices Regulation (MDR), it became apparent that manufacturers should assign UDI to medical devices. This is intended to allow the identification and to improve the traceability of devices, as well as to provide monitoring and to run the fighting mechanism against medical device counterfeiting. The whitepaper discovers UDI requirements, implementation process and benefits.
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Data integrity, Good Manufacturing Practice (GMP), Manufacturing, Medical Devices, Packaging, Regulation & Legislation, Supply Chain