Feasibility for CRO
Worldwide feasibility studies
Study start-up: site identification, qualification, and selection
Contract management
Regulatory documents development and review
Study documents development
Conduction of training for Investigators
Essential document collection
Trial Master File set-up and maintenance
Site monitoring and management (on-site and remotely)
Subject recruitment and retention
Conducting training for Clinical Research Associates
Site initiation, monitoring and close-out
On-site source data verification
Medical monitoring
Sponsor liaison
Audit preparation
IRB/EC submissions
Third-party vendor management
Your Gateway to High-Performance Clinical Trials in Ukraine
For US and EU-based CROs, selecting the right Eastern European sites is a high-stakes decision. Ukraine Research Lab LLC provides expert, boots-on-the-ground Feasibility services in Ukraine, bridging the gap between Western standards and local medical infrastructure.
Why Ukraine? Why Now?
Despite global shifts, Ukraine remains a powerhouse for clinical research due to:
Centralised Patient Databases: Rapid identification of large, treatment-naïve populations.
High Investigator Engagement: Motivated, GCP-certified medical professionals.
Cost-Efficiency: Significant reduction in per-patient costs without compromising data quality.
Our Specialised Feasibility Services
We don't just send questionnaires; we provide actionable intelligence.
Rapid Site Identification: We maintain an active database of "Rescue Sites" and top-tier clinical centres across all therapeutic areas.
Regulatory Intelligence: Up-to-the-minute tracking of State Expert Centre (SEC) and Ethics Committee timelines.
Protocol Stress-Testing: We evaluate your protocol against local Standards of Care to ensure zero friction during recruitment.
On-Site Validation: Physical verification of equipment (e.g., cold chain storage, centrifuge specs) and staff capacity.
Bridging the Gap: US/EU Standards, Local Expertise
We operate with a Western mindset. Our reports are delivered in English, formatted for immediate inclusion in your Sponsor presentations, and backed by the ALCOA+ principles of data integrity.
We minimise your "Non-Performing Site" rate by identifying the hurdles before the first patient is even screened.