Representing and mapping Australia’s capacity and capability for effective device testing is hugely important. You can find information on our growing network through our main menu above.
Our network includes traditional specialists, including CROs, clinical sites and investigators as well as relative skill gaps in Australia, including health economists, bioengineers and designers.
If you’re testing a Cardiovascular-focused medical device and looking for partners or solutions, Ventri Clinical can connect you to globally renowned specialists in Australia.
Suited to any all stages of clinical development, Ventri’s network benefit’s from it’s facilitation by the Australian Cardiovascular Alliance, the country’s industry peak body for clinicians and investigators.
Ethics & Regulatory
To obtain access to the Australian market, medical device and IVD manufacturers will need to include their product in the Australian Register of Therapeutic Goods (ARTG), regulated by the Therapeutic Goods Administration (TGA). Each of the Australian states and territories also have separate legislation relevant to the conduct of clinical trials. Investigators, HRECs, approving authorities and trial sponsors should ensure that they comply with the specific requirements for each jurisdiction.
Ventri Clinical can support your pathway through any stage of trialling or product launch.
Ventri Clinical can help connect and manage multiple service providers, clinicians, sites or experts for testing projects or studies. Partnered with some of the most experienced and successful investigators in the hemisphere, we’re best placed to support, consult and help manage device testing.