Regulatory update from the Medical Devices Surveillance Branch
Presented at the ARCS Annual Conference 2024. Regulatory Update from the Medical Devices Surveillance Branch-Medical Devices Vigilance Program and Mandatory Reporting of Adverse Events by Healthcare Facilities.
Date
Related content
-
Unique Device Identification (UDI) information session for clinical quality registries
This information session introduces UDI for clinical quality registries. Australia’s UDI framework supports improved identification of medical devices and in vitro diagnostic (IVD) devices.