NMPA issued the notice “Soliciting Feedback of Guideline on Medical Device Human Factors Design for the Second Time” on October 11, 2023, after the first round released in May 2020. The feedback needs to be submitted by October 30, 2023.
This proposed guideline applies to the human factors design and usability engineering of Class II and III medical devices but does not apply to in vitro diagnostic reagents. It refers to international regulations such as FDA’s “Applying Human Factors and Usability Engineering to Medical Devices” and “List of Highest Priority Devices for Human Factors Review”, etc.