They’re Here: New Draft European Medical Device & IVD Regulations Published

European lawmakers and regulators have published eagerly awaited draft versions of new medical device and IVD regulations earlier than anticipated.

Emergo consultants in Europe and the US are performing a comprehensive evaluation of the newMedical Device Regulations (MDR) and In VitroDiagnostic Regulations (IVDR) to determine any significant changes from initial proposed regulatory changes in 2012.

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