PERTH, Australia – Six classes of medical devices listed on Australia’s Register of Therapeutic Goods (ARTG) will fall under new classification requirements on Nov. 25, 2021, following numerous consultations with industry. The consultations were part of the Australian government’s plans to overhaul its medical device regulations to be more in line with the European Medical Device Regulation (MDR).
BioWorld MedTech Regulatory Asia-Pacific Australia TGA"device" - Google News
May 19, 2021
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TGA wraps up device reclassifications, extends deadlines for six groups of medical devices - BioWorld Online
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