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Cooperation possibilities
Managing contracts governing the transfer of clinical data and biological specimens, response to adverse events, overseeing documented cases and clinical recommendations, facilitating research collaborations, medicinal product development and final report submission to Regulatory Authorities.
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- Zoltan SAGI
Some insights
We accelerate life-changing clinical research by delivering high-quality, compliant and compassionate CRO services across Europe. We connect sponsors with patients faster, broaden access to innovative therapies and uphold the highest ethical standards to improve global health.
I’m proud of our passionate team of experts – from PIs to research nurses – delivering compliant, efficient, compassionate clinical trials across Europe. Our focus on quality, patient well-being, and faster access to innovative therapies drives better health outcomes.
Current strengths: experienced PIs, CRAs and PMs; GCP/EMA compliance; CEE network (7 countries, 290+ sites); risk-based & decentralized trial expertise; patient-centric care. Future: advanced biostatistics & data management, AI-driven monitoring, digital eClinical tools.
"He is always on the phone with medicine bosses, planning tests for new drugs in places like Hungary, Czech Republic and Poland. Figures out the rules, money, and calendars, then hurries home so we can eat dinner together."
By collaborating with Swiss KoLs and Sponsors, we can co-develop innovative therapies, leverage eClinical platforms and CEE PI networks, and integrate advanced biostatistics and AI tools for faster, data-rich trials that benefit patients and stakeholders alike.
I’d welcome introductions to CxOs at sponsor organizations eager to launch clinical trials in Central and Eastern Europe.