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Home » TGA Issues Guidance on Device Conformity Assessments During COVID-19
TGA Issues Guidance on Device Conformity Assessments During COVID-19
Australia’s Therapeutic Goods Administration (TGA) said that, in light of delays due to the COVID-19 pandemic and limitations on the number of notified bodies designated under the European Medical Devices Regulation, devicemakers could see their conformance assessment documents lapse for their listed devices on Australia’s Register of Therapeutic Goods.
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