The IMDRF is a voluntary group of medical device regulators from around the world whose mission is to strategically accelerate international regulatory convergence, promoting an efficient and effective regulatory model for medical devices that is responsive to emerging challenges in the sector while protecting and maximizing public health and safety.
The decisions on behalf of the IMDRF are made by a Management Committee (MC) that is responsible for “provides strategic direction; identifies and prioritizes regulatory challenges to be addressed; determines the implementation process and monitors the work plan; and authorizes resources in support of advancing IMDRF’s goals and objectives.”
The current members are:
- South Korea, and
- the United States of America.
You can access the IMDRF website here