EU: New MDCG document Q&A on custom-made devices

The MDCG has published a new document on custom-made devices. This Q&A is a high-level document aimed at addressing the most pertinent questions relating to custom-made devices falling under Regulation (EU) 2017/745 on medical devices (MDR).

You can find this document here: MDCG 2021-3 – Q&A On Custom-Made Devices

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