Global Medtech Guidance Tracker: January 2022

Stay current on regulatory guidelines from around the world with Medtech Insight's Guidance Tracker. Thirty-eight documents have been posted on the tracker since its last update.

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Thirty-eight guidance documents on medical devices and diagnostics issued by regulatory authorities from around the world were added to Medtech Insight’s Guidance Tracker in the past month.

The updated tracker includes new guidance from the European Commission’s Medical Device Coordination Group explaining how sponsors should collect and maintain clinical evidence for diagnostic tests under the EU IVD Regulation

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