Elephants depend on the senior female, the matriarch, to share her experience for their family group survival. At Gaea, we share our experience of 28 years to bring a Sponsor’s clinical trial to a timely, cost-effective completion, with quality at the core. Gaea OÜ is an agile, flexible, full-service CRO with only highly experienced staff. Inspired by the iconic elephant, we also support their conservation in Kenya. Our corporate office is based in Tallinn, in digital Estonia. We set up and manage Phase I – III trials and any tasks agreed for IIT in all of Europe, UK, USA and Georgia, with partners in Bangladesh/Nepal, East/South Africa and our affiliate in Korea (Gaea APAC). Our approach of using our qualified service providers, such as data management, means we can supplement individual Sponsors, that may also have their own preferred providers, with our own as they need. Critically, with all under our umbrella of project management so the Sponsor has one contact point. Our range of expertise is in hospital-originated interventions. We usually work with limited populations, rare or difficult oncology populations, and intensive care populations where trials enrol over 24/7 and require deeply committed CRO team. Our experience includes oncology/hematology, infectious diseases, microbiome, intensive care. Our experienced CPM are actively engaged in the day-to-day details of a clinical trial. The CPM is the go-to person for the providers and the point of contact for the Sponsor, keeping communication fast and direct. We only have senior staff in HQ. National CRAs in each country, who are responsible for regulatory submission to EC (LEC) and CA, usually have 15-20 years of experience. In the most complex countries, we include a National Regulatory Manager. Our staff is strictly keeping up-to-date with regulations. CPM and CEO have extensive experience in regulatory and ethics. The skills of experienced CTM and In-House CRA are also applied to each project.