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Home » Australia’s device reforms mostly completed, but postmarketing efforts take central stage
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Australia’s device reforms mostly completed, but postmarketing efforts take central stage

Dec. 31, 2021
By Tamra Sami
PERTH, Australia – Australia’s Therapeutic Goods Administration (TGA) has undertaken a massive effort to reform its drug and device regulations, and as it pulls into the homestretch with those reforms, it is setting its sights to postmarketing efforts that include adverse event reporting, conformity assessments, patient-reported outcomes and a universal device identifier program.
BioWorld MedTech Regulatory Asia-Pacific Australia TGA

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