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APAC’s Strategic Advantage in Oncology Trials

Presented by Teresa Ringeri, Director, Business Development & David Fuller, Oncology Medical Advisor

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Expo Summary

At a recent industry event, Southern Star Research’s experts Teresa Ringeri and David Fuller presented insights into the growing importance of the Asia-Pacific (APAC) region in oncology clinical trials. Their presentation, “APAC’s Strategic Advantage in Oncology Trials: Fast Start, Lower Cost, Global Impact,” highlighted why global biopharma companies are increasingly turning to the region for their early and late-phase studies.

Key points from the presentation include:

  • Faster Study Start-Up: APAC countries, including Australia and South Korea, offer streamlined regulatory processes and strong institutional networks, enabling quicker site activation and patient recruitment.
  • Cost Efficiency: Operational costs in APAC are significantly lower compared to the US and EU, without compromising trial quality or timelines.
  • Global Relevance: The region’s diverse patient population, experienced investigators, and world-class infrastructure ensure that data from APAC trials are widely accepted by regulatory agencies worldwide.

Southern Star Research’s proven experience in managing complex oncology studies across APAC provides sponsors with a reliable partner to navigate the region’s regulatory and operational landscape. Our local expertise, combined with global trial oversight, ensures that oncology programs are delivered efficiently and with high data integrity.

Media Contact

Simi Barretto

Marketing and Digital Media Manager
Southern Star Research
Location: Australia
Email: media@southernstarresearch.com

Head Office:

L1, 1 Merriwa Street,

Gordon, NSW, 2072 Australia

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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.

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