Australia is the world’s fastest growing destination for clinical research due to its high quality facilities, globally-renowned CROs and the government R&D tax incentive scheme.
The global portability of Australian clinical data (>70% of all FDA submissions have some Australian data within them since 2019)
The speed to commence clinical trials in Australia (typically under 8 weeks)
The sheer cost savings as compared to the USA, EU or UK (typically half the price or less)
The access to the Australian Government R&D Tax Incentive which is up to a further 43.5% cash rebate on all research costs for work performed in Australia
Australia’s Clinical Research Organizations (CROs) are renowned for their expertise, innovation, and commitment to delivering high-quality clinical research services.
Contract Development and Manufacturing Organizations (CDMOs) in Australia play a pivotal role in the pharmaceutical supply chain by offering specialized services that encompass the design, development, and manufacturing of drugs.
Australia has high quality bioanalytical labs, which are FDA Audited, NATA accredited and GLP compliant.
Australia hosts a diverse range of clinical trial sites that are equipped to handle the complexities of both early and late-phase studies.
Australia’s largest phase 1 clinical trial site, with a focus on early-stage clinical development.
Australia has high quality bioanalytical labs, which are FDA Audited, NATA accredited and GLP compliant.
Venture capital investment in life sciences within Australia is vibrant and critical to the growth of innovation in biotechnology and healthcare. Australian life science VCs are active in nurturing startups and established companies alike, providing not only capital but also strategic guidance and access to international networks.