QMSR: Industry wants to avoid ISO 13485 ‘plus,’ seeks longer transition period
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Audit/FDA InspectionDiagnosticsMedical DevicesNorth AmericaProduct LifecycleRegulatory Intelligence/PolicyRegulatory NewsMichael MezherAudit/FDA InspectionDiagnosticsMedical DevicesNorth AmericaProduct LifecycleRegulatory Intelligence/Policy