Medical Device Information Analysis and Sharing Initiative (MDIAS)
MDIAS is a voluntary partnership between the FDA and the private sector formed to proactively analyze broad and extensive medical device-related data to improve healthcare outcomes for patients.
The MDIAS community currently includes a subset of the medical device ecosystem – device manufacturers, healthcare providers, and the Food and Drug Administration – that contribute time, expertise, and data to the effort. Select one of the groups below to learn more about how to be involved.
Learn more about how the MDIAS study results contribute to advancing device quality and ultimately, patient safety.