FDA aims to clarify device malfunction summary reporting requirements
Regulatory NewsFerdous Al-Faruque
ComplianceDiagnostics/IVDsEthicsMedical DevicesNorth AmericaProduct LifecycleQuality Assurance and ControlRegulatory Intelligence/PolicyRegulatory NewsFerdous Al-FaruqueComplianceDiagnostics/IVDsEthicsMedical DevicesNorth AmericaProduct LifecycleQuality Assurance and ControlRegulatory Intelligence/Policy