Collaborate with top-tier European research sites to accelerate patient recruitment, reduce trial costs, and improve operational timelines.
We help sponsors access GCP-compliant centers across Eastern Europe with clarity, speed, and reliability.
We match sponsors with suitable research sites across Romania and Eastern Europe. We identify and pre-qualify clinical research sites that fit your protocol, patient population, and operational needs.
Each site is assessed for GCP compliance, infrastructure, investigator experience, recruitment history, and feasibility potential.
You receive a curated shortlist tailored to your study’s objectives.
We collect operational metrics and ensure all sites comply with ICH-GCP standards. We conduct structured feasibility assessments to ensure sites can deliver on timelines and recruitment targets. Our process covers operational metrics, staffing, equipment, past trial performance, and regulatory readiness. Sponsors receive transparent evaluations to support confident site selection and early-stage planning.
We facilitate communication and early coordination between sponsor and site teams.
This includes introductions, study interest validation, document exchange, and alignment on timelines and expectations.
Our goal is to streamline the placement process so studies can initiate smoothly and without delays.
Eastern Europe offers a unique combination of fast recruitment, competitive costs, and highly skilled investigators.
Romanian research centers deliver strong performance across oncology, internal medicine, infectious diseases, and metabolic disorders — all within a fully GCP-compliant environment aligned with EMA standards.
Faster patient recruitement
Lower per-patient costs
Highly motivated investigators
Strong oncology and internal medicine capabilities
Fully GCP-compliant regulatory environment
EuroPartner Trials is a boutique consultancy connecting Western European sponsors with high-quality clinical research sites in Eastern Europe.
Based between Belgium and Romania, we provide localized insight, fast communication, and transparent site engagement.
Our mission is to simplify the site identification and feasibility process while maintaining the highest standards of compliance and operational excellence.
We collaborate with a growing selection of research centers and continuously expand our network based on sponsor needs. All sites are pre-evaluated for GCP compliance and operational readiness.
Yes. Only ICH-GCP compliant and EMA-aligned sites are considered. We verify investigator credentials, facility standards, and documentation practices.
Oncology, internal medicine, infectious diseases, metabolic diseases, gastroenterology, neurology, and more. We adapt site selection to your protocol and patient population.
Regulatory oversight remains with the sponsor and the selected site.
We support the early coordination required to ensure all processes meet local and international standards.