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Reforms in the medical devices regulatory framework

8 March 2011

Late last year, the Therapeutic Goods Administration – or TGA –  called for comments on a discussion paper on proposed changes to the third party conformity assessment for medical devices, amendments to the way in which a medical device is included on the Australian Register of Therapeutic Goods and enhancements to the identification of approved devices.

Submissions on this discussion paper have now been made public.  You can read Medtronic’s submission here.

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