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Implementation Timelines Set for Trans-Tasman Authority

March 26, 2012
Australia and New Zealand will begin sharing device and drug good manufacturing practice reports shortly, with the aim of establishing joint GMP audit capability by early 2013 — part of a much larger plan to merge the countries’ health products regulatory authorities. The goal is one of five to be completed over the next year, according to Australia’s Therapeutic Goods Administration (TGA) and New Zealand’s Medicines and Medical Devices Safety Authority (Medsafe).
International Medical Device Regulatory Monitor