TGA struggles with severe understaffing as medical device adverse events surge
Australia's medical device regulator, the Therapeutic Goods Administration, is severely understaffed to handle adverse event reports from 1.4 million devices in use. The TGA's monitoring team operates at only 50 percent capacity despite expecting a tenfold surge in alerts after mandatory hospital reporting began in March 2024.
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Published 02 Aug 2026, 09:52 UTC · Updated 02 Aug 2026, 10:00 UTC
Summary by OZbrief Editorial. Original report: SMH. Editorial policy · Corrections
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