Joseph Cox
Manager, Business Development
Manager, Business Development
Meet us at the BIO-Europe Spring 2026
23–25 March 2026
Lisbon, Portugal
Southern Star Research is excited to attend the BIO-Europe Spring 2026 – that will bring the global life sciences community together in Lisbon for three days of in-person partnering, followed by two days of digital meetings. As part of Spring Innovation Week, the event focuses on building practical collaboration that support research, development, and commercial growth across biotechnology and pharmaceuticals.
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 the BIO-Europe Spring 2026?
BIO-Europe Spring is designed for investors, biotechnology leaders, and pharmaceutical business development teams seeking focused and efficient partnering. The event combines one-to-one partnering meetings with plenary sessions, company presentations, and informal networking.
The conference attracts thousands of participants from more than 60 countries, representing biotech companies, pharmaceutical organisations, investors, and service providers. A high volume of pre-scheduled meetings helps attendees use their time effectively and concentrate on relevant discussions.
At BIO Europe Spring 2026, you can:
Connect with our team at the BIO Europe Spring 2026
Fill out the form to schedule a meeting with our team and learn how Southern Star Research can support your clinical development objectives across the Asia-Pacific region.
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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.