Study: Nearly one-third of device adverse event reports were late or missing data
Regulatory NewsMary Ellen Schneider
Adverse eventsMedical device reportingMedical DevicesPharmacovigilance/postmarket surveillanceProduct LifecycleUnited StatesRegulatory NewsMary Ellen SchneiderAdverse eventsMedical device reportingMedical DevicesPharmacovigilance/postmarket surveillanceProduct LifecycleUnited States