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AMA submission on TGA proposals to align Australia's medical device regulations with European regulations

12 Oct 2017

The AMA supports a comprehensive product vigilance system in line with international best practice​.​  The AMA therefore fully supports the TGA’s plans to bring Australia’s medical device regulations in line with European regulations, including the requirement for patient implant cards and information leaflets to accompany all implantable medical devices.


Published: 12 Oct 2017