Increasingly, sponsors turn to Australia for clinical trials, as the country promises rapid approval times, high-quality research, and world-class health infrastructure. However, the cost of clinical trials in Australia is also a major drawcard. Today, we delve into the factors contributing to this phenomenon, shedding light on why conducting clinical trials in Australia is a smart choice for researchers and sponsors alike.
One key factor that makes clinical trials in Australia cost-effective is the Research and Development (R&D) Tax offset, which is your corporate tax rate plus an 18.5% premium. This incentive encourages companies to engage in research and development activities, including clinical trials, by providing a generous offset on eligible R&D expenditures. This financial boost significantly reduces the overall cost burden of your study, making Australia an attractive destination for clinical research.
Australia’s competitive cost structure and the availability of state-of-the-art research infrastructure further contribute to cost savings. The country’s healthcare system, emphasizing efficiency and uncompromising quality, helps you receive excellent value for your investment.
Did you know that trial start-ups in Australia can be up to 4-6 months faster than in the US? This is because Australia’s clinical trial landscape benefits from a straightforward regulatory process, with the Clinical Trial Notification (CTN) scheme playing a pivotal role. The CTN scheme can expedite your clinical trial startup by reducing regulatory friction to kickstart your research.
This scheme enables you to notify regulatory authorities of their intent to conduct a clinical trial, streamline the approval process, and accelerate your study from end to end.
While cost-effectiveness is a significant advantage, Australia does not compromise on the quality of clinical trials. There is a steadfast commitment to scientific efficacy and ethical conduct, ensuring that you obtain meaningful and reliable results from your trial. This commitment reduces the likelihood of having to redo work due to compromised integrity, ultimately saving both time and resources.
Australia’s stringent regulatory framework, overseen by bodies such as the Therapeutic Goods Administration (TGA), ensures that clinical trials adhere to the highest standards. This means that ethical considerations are top priority throughout your research process, promoting participant safety and data integrity the whole way through.
The low cost of clinical trials in Australia is not a coincidence but the result of a strategic blend of financial incentives, streamlined processes, and an unwavering commitment to scientific excellence. For sponsors seeking a cost-effective, efficient, and high-quality environment for their clinical trials, Australia emerges as a promising opportunity. As the global clinical research landscape continues to evolve, Australia’s unique combination of advantages positions it as a frontrunner in the medical research space.
If you want to learn more about how you can successfully and cost-effectively navigate clinical trials in Australia with a team of committed professionals, get in touch with us today.
Southern Star Research is your full-service CRO with broad therapeutic expertise and deep local knowledge to help you conduct clinical trials in Australia and the Asia Pacific. Our seasoned experts offer a tailored approach to every project while ensuring compliance and scientific efficacy. If you’re looking for a knowledgeable and dedicated team to help you run a successful trial in Australia or APAC, contact us today.
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Each member of our Leadership Team boasts an average of 30 years experience. Our clients have access to an extraordinary group of Clinical Research professionals, whose experience covers Multinational Pharmaceutical companies, Biotechnology, Medical Device, CRO’s, research institutes, Universities, Industry Associations & Government Bodies. Together, we ensure that every aspect of your unique and novel drug study clinical trial is handled with scientific precision, care, and foresight.
Our team has all of the tools, knowledge and experience to solve almost any issue that may arise during the complex clinical trial process.
We recognize that each study is unique and different and there are nuances that need to be resolved proactively.
Our advisory board of top-tier specialists in multiple therapeutic areas engage in the early stages from protocol design in constructive discussions to anticipate challenges and enhance study efficiency throughout the study.