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