Speed, Quality & Cost – Conducting Your Clinical Trials in Australia

Watch our webinar about why you should be conducting your Clinical Trials in Australia and find out more about trial design, R&D incentives, eligibility and more.

Watch PCI Clinical Services and their partners for this educational webinar to learn more the specific considerations required for Phase I trial design in Australia. You’ll also discover Australia’s R&D tax incentive program and eligibility when conducting your trials in Australia, alongside the specific requirements for importing, manufacturing, compounding and labelling your product for Australian clinical studies.

Over the last 20 years, Australia has grown to become a destination of choice for the conduct of early phase clinical trials. Rapid ethics approval and a simple notification to the Therapeutic Goods Administrations (TGA) means that from submission to FPFD it will only take on average 6 weeks. Coupled with the attractive R&D tax incentive program offered by the Australian Government, this swift pathway to study data can then be used to support an IND or IMPD application allowing companies to speed up their drug development process.

Speakers:

Cameron Johnson, Chief Executive Officer and Managing Director, Nucleus Network Ltd.

Cameron Johnson joined Nucleus Network in August 2013 as the Chief Operating Officer, before moving into the position of Managing Director. Prior to joining Nucleus Network, Cameron held the position of Chief Executive Officer at a Phase 1 Clinical Trials Organisation and was also the inaugural CEO of the company. Cameron has worked in early phase clinical trials organisations across Australia and Europe since 2001.

Craig Rogers, SVP of Asia Pacific, PCI Clinical Services.

Craig has over 20 years of experience working within the pharmaceutical industry. This included roles in Regulatory Affairs at big pharma and local biotech; Scientific Affairs at IDT; and General Manager at both CMAX and Nucleus Network Phase I clinical units. In 2008, Craig established PPP, based on his gap analysis of the services available in the local market, to support clinical trial manufacturing and logistics. Craig is a registered pharmacist, toxicologist and lawyer.

Simone Quin, Partner, Prime Accounting and Business Advisory Services.

Simone has over 20 years of experience in the business management of science and research, including positions within universities, government, collaborative research centres and in consulting. Simone has a Bachelor of Commerce degree from the University of Melbourne and a Graduate Certificate in Science and Technology Commercialisation from Adelaide University; a Graduate Diploma in Applied Corporate Governance and is a member of the Institute of Chartered Accountants.

Please feel free to contact the PCI team talkfuture@pciservices.com

Watch the webinar below.



As well as Clinical Trials in Australia we support our customers with complete Clinical Trial services

PCI is committed to supporting clients at every stage of the of the clinical cycle, delivering best-in-class services efficiently and effectively. Our clients come to us seeking solutions to often complex and unique opportunities due to our reputation in offering unmatched flexibility, a client-centric experience and consultative approach.

Find out more about our clinical trial services here

When it comes to pharmaceutical and biopharmaceutical supply chain expertise who do you trust?

Your bridge between life-changing therapies and patients