Medical device adverse event monitoring update - June 2025
An update about expected increases in the number of medical device incident reports reported to the TGA
Published
Related content
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New regulations to strengthen medical device patient safety
Australians who rely on medical devices will benefit from new measures introduced by the Australian Government to enhance the identification and management of device-related safety concerns. -
Making therapeutic goods safer for everyone
One of the key functions of the Therapeutic Goods Administration (TGA) is to closely monitor the safety of therapeutic goods. But to properly monitor safety, we need everyone to report any side effects and problems they have. -
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