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MDR

Thursday, February 13th 2025

News

European Medicines Agency Q&A guidance on the implementation of the MDR and IVDR update

The EMA has updated its Q&A guidance on the implementation of EU regulations for medical devices and in vitro diagnostic medical (...)

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Thursday, October 31st 2024

News

Updated Draft Statutory Instrument for Post-Market Surveillance: Gap Analysis

A new draft statutory instrument for post-marketing surveillance has been published. Our team has conducted a detailed gap analysis to (...)

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