Forty-two 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 several guidance documents to support the implementation of the EU In Vitro Diagnostics Regulation (IVDR) that became applicable on 26 May. Among others, there is a notice from the European Commission marking the end of the mutual recognition agreement between the EU and Switzerland in relation to IVDs
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