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Medical device incident reporting & investigation scheme (IRIS) articles

The IRIS is responsible for the management of all reports of adverse events or problems associated with medical devices that are reported to the TGA.

Between 2001 and 2009, IRIS safety alerts and statistics were included as an insert in TGA News. Prior to this they were part of the Australian Therapeutic Device Bulletin.

There is also an IRIS article index alphabetised according to device type, product name and issue.