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