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Synergy Global Ukraine is an international full-service Contract Research Organization headquartered in Ukraine, with on-the-ground representatives in Canada, North America, Mexico, Poland, France, Italy, the United Kingdom, Serbia, Romania, Lithuania, Croatia, Latvia and Georgia.
With 13+ years of hands-on experience in planning and executing full-cycle Phase I–IV clinical trials, we confidently handle projects of any complexity. Most of our portfolio includes oncology, respiratory, cardiology, neurology and gastroenterology studies, though our expertise spans many other therapeutic areas as well.
We closely monitor global industry trends and regulatory developments, consistently implementing best practices while combining global thinking with precise local execution. Our team understands the geographical, economic, cultural and infrastructural nuances that shape clinical research – and adapts quickly and intelligently to each environment.
We conduct clinical trials either fully in-house or as a trusted regional partner within international multicenter programs. Our flexible operating model allows Sponsors to choose the level of collaboration they need – whether it’s full outsourcing or seamless integration into existing global frameworks.
With access to extensive reference patient databases and a wide network of highly experienced Principal Investigators, we ensure efficient site selection, rapid enrollment and consistent protocol compliance. Our operational footprint spans Ukraine, Canada, North America, Mexico, Poland, France, Italy, the United Kingdom, Serbia, Romania, Lithuania, Croatia, Latvia and Georgia – providing Sponsors with diverse patient populations and resilient clinical capabilities.
Synergy Global Ukraine has established a structured, high-performance clinical environment that supports all phases of research. Our investigators, clinical sites and medical experts work as an aligned ecosystem. This enables several things – Accelerated patient recruitment, Reliable, high-fidelity data collection, Robust adherence to international standards, and Streamlined oversight and real-time decision-making.
Across all regions, we generate data that align with the expectations and formatting standards of major global regulatory authorities, including:
FDA, EMA, MHRA, Health Canada and other international agencies.
This ensures that every dataset we deliver is inspection-ready, consistent, and fully suitable for global submission pathways.