Australian TGA sets new regulations for permanently implantable medical devices

By Stewart Eisenhart, Emergo Group

The Australian government is set to begin requiring new market registrants of some implantable medical devices to provide detailed consumer information leaflets with their products on December 1, 2018 as part of a broader effort to align Therapeutic Goods Administration (TGA) regulations with the European Medical Devices Regulation (MDR).

Get the full story here at the Emergo Group’s blog.

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