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Medsafe and Therapeutic Goods Administration (TGA) discussion document - joint regulatory scheme for therapeutic products under ANZTPA

The Therapeutic Goods Administration (TGA) and Medsafe are seeking comments and input from interested parties on a discussion paper setting out the high level features of a possible framework for regulation of therapeutic products within the ANZTPA-a joint scheme to regulate therapeutic products in Australia and New Zealand.  The draft discussion document focuses on the manufacture and approval of medicines, medical devices and blood & blood components biological.

Consultation document in PDF - 372kb

Consultation document in Word - 115kb

NZNO will be making a submission if you wish to provide feedback please send it to Leanne Manson Policy Advisor;

Feedback Due: 15 February 2013

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