Accell Clinical Research is an international full-service Contract Research Organization (CRO) managing Phase I-III clinical trials for 15+ years across Europe and Eurasia. With a local presence, including highly qualified medical staff and legal entities in the region, we successfully recruit patients both in the EU and outside the EU in post-Soviet countries (CIS). All together we provide guaranteed fast patient recruitment in 20+ countries across the region.
⬇︎ ACCELL'S SERVICES for Phase I-III clinical trials:
• Strategic guidance and trial set-up:
• Feasibility research and site selection
• Study documentation development
• Regulatory support
• Clinical supply import and management
• Selection and management of clinical study vendors
• Project management
• Clinical & medical monitoring
• Data management and biostatistics
• Quality assurance
• Safety management
• TMF/eTMF services
• Functional outsourcing of a clinical team
⬇︎ THERAPEUTIC AREAS
• Oncology
• Cardiovascular
• Immunology
• Gastroenterology
• Neurology
• Endocrinology
Specialized CRO Services for Biotech & Pharma -
For over 20 years, PRC Clinical has delivered high-quality clinical trial execution with a high-touch, specialized approach. We combine deep therapeutic expertise with innovative solutions, ensuring trials run efficiently while maintaining the highest standards of care.
With a strong foundation in Phase I trials and extensive experience in CNS, regenerative medicine, and ophthalmology, we provide:
-Site Selection & Management – Partnering with top sites for optimal recruitment & retention.
-Project Management – Ensuring timelines, budgets, and compliance stay on track.
-Accelerated Enrollment Strategies – Proven methods to drive successful patient recruitment.
-Technology-Enabled Clinical Operations – Real-time data insights for better trial outcomes.
PRC Clinical continues to set new standards in clinical operations, regulatory compliance, and sponsor success.
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