APEC Regulatory Harmonization Steering Committee (RHSC)
Results
Working group
Review the GHTF NCAR Exchange Program and to advise on opportunities for improvement
Working group
Leverage regulatory resources to manage an efficient, effective, and sustainable single audit program.
Working group
Development of non-binding rules for creating, using, and maintaining unique device identifiers and related activities.
Working group
Registries of patients undergoing medical device procedures represent a growing potential electronic resource for local and global medical device evaluation and tracking.
Working group
Initiatives undertaken on behalf of the IMDRF Management Committee
Working group
A working group for Clinical Evidence for IVD Medical Devices
Working group
Promote consistency in regulatory assessment for Software as a Medical Device to reach patients more efficiently.
Working group
Seeking to harmonize internationally, principles to help promote the development of safe and effective AI/ML enabled medical devices
Working group
Ensure alignment of IMDRF QMS and risk management documents with current international standards