Finally the latest unapproved drugs, and medical devices are within the reach of Category A terminal patients.
This applies to the TGA (Therapeutic Goods Administration) which are the Federal Government body that are the Australian equal to the FDA in the US.
The Patients Medical practioner has to prescribe the experimental treatment and the researcher is then allowed to sponsor the Device or Drug before approval.
This is only for Cat A patients who are likely to be terminal without intervention.
Australia may be a fair distance away but as a last option this would surely be an option for many that can afford the air fair.