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Meet us at BIO Europe

November 3-5, 2025
Vienna, Austria
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Meet us at BIO-Europe

November 3-5, 2025

Vienna, Austria

Digital Partnering – November 11-12, 2025

Southern Star Research is excited to attend the upcoming BIO-Europe Global Biopharma Partnering Event 2025. BIO-Europe Conference is an annual life sciences partnering event that helps connect professionals in the industry to drive innovation.

Southern Star Research is a full-service Contract Research Organization (CRO) specializing in early-phase clinical trials and navigating the complexities of bringing new medical products to market. Our global network of experts delivers high-quality services across medical writing, clinical monitoring, project management, biostatistics, data management, safety and medical monitoring, and quality assurance.

Why connect with Southern Star Research at BIO-Europe 2025?

  • Benefit from local and global experience in clinical research and regulatory support
  • Take advantage of Australia’s fast approval pathways and generous R&D tax incentives
  • Access strong early phase trial capabilities, including healthy volunteer studies
  • Expand into APAC with local insights and established regional partnerships

About BIO-Europe 2025

BIO-Europe 2025 is one of the leading global events for biotech and pharma collaboration, bringing together over 5,700 attendees from more than 60 countries. With 30,000+ one-on-one meetings expected, this conference offers unmatched opportunities to connect, learn, and grow. Virtual meetings will remain available through November 11–12.

At the BIO-Europe 2025, you can:

  • Connect through high-value in-person and virtual partnering meetings
  • Explore strategies for custom trial designs, operational support, and cost efficiencies
  • Gain insights into investment trends, AI applications, and global partnerships
  • Discover the latest innovations transforming the life sciences industry

Connect with our team at BIO-Europe 2025

Fill out the form to schedule a meeting with our team and learn how Southern Star Research can help you achieve your clinical trial goals.

Schedule a meeting

BIO Europe 2025 GF

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The Australian Advantage

Cost

Eligible organisations receive a 43.5% cash rebate on trial costs with the Australian Research & Development tax incentive.

Speed

Get you trial up and running in 8 weeks with streamlined ethics approvals and no need for an Investigational New Drug application.

Quality

World-class healthcare facilities and renowned experts ensure your data is accepted by international regulatory bodies like the FDA and EMA.

Come and meet us

Our team will be available throughout this event to discuss how we can support your research initiatives. Whether you’re looking to start a new project, save an existing one or simply explore new partnership opportunities, we’re here to help.

Dr David Lloyd

Managing Director

  • 30 years of research experience in academia, pharma & CROs
  • Advisor to the Australian Government on Clinical Research reforms
  • Prominent industry positions including Co-Chair of the R&D Taskforce
  • Appointed to NSW Dept of Health Early Phase Expert Oversight Committee
  • Previous member of several NHMRC committees overseeing clinical research

 

Dan Evans

Daniel Evans

Director, Business Development

  • Located in Sydney, Australia
  • 10+ years of experience in biotech consulting and CRO industry
  • Strong expertise in global business development for biotech and pharma
  • Deep understanding of biotech needs and challenges
  • Extensive experience in partnering with global biotech to deliver fast, cost-effective, high-quality clinical trial.
Head Office:
Phone: +61 2 9011 6266

L1, 1 Merriwa Street,

Gordon, NSW, 2072 Australia

E: info@southernstarresearch.com 

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Specialist experience

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.